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Field of expertise:	All Health Economics and Financing    Cost-effectiveness Studies    Costing Studies    Health Expenditure Review    Health Financing and Provider Payment    Health Insurance    National Health AccountsHealth Programmes    Basic Health Services    HIV-AIDS-STI-TB    Hospital Services    Other Health Programmes    Reproductive HealthHealth System    Health Information System / Epidemiology / Operational Research    Health Policy and Policy Dialogue    Health Sector Reform    Health Sector Review or Health Sector Diagnosis    Monitoring and Evaluation    Planning, Organisation and Management    Public Private Partnership    Sector Wide Approach (SWAp)    Training and Human Resource DevelopmentPharmaceutical Sector    Access to Medicine Campaigns    Drug Pricing Studies    Drug Regulatory Authority Support    Drug Supply Management System Strengthening    Essential Drugs Programme Support    Essential Medicines Financing    Increasing Transparency In Public And Private Pharmaceutical Markets    Medical Store Evaluation    National Medicines Policy Development    Pharmaceutical Sector Review    Procurement and Tender Support    Public Private Partnership Interventions    Quantification of Essential Drug Needs    Rational Use Surveys    Selection of Essential Medicines    Training and Human Resource DevelopmentProject Cycle    Appraisal    Identification and Formulation    Long Term Technical Assistance    Monitoring and Evaluation
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Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Bahamas
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Barbados
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Antigua and Barbuda
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Caribbean Partnership
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Dominica
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Dominican Republic
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Grenada
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Haiti
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Jamaica
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Montserrat
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	St. Kitts and Nevis
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	St. Lucia
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	St. Vincent and the Grenadines
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Trinidad & Tobago
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Belize
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Suriname
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Drug Regulation and Regulatory Systems
Client:	Caribbean Community (CARICOM) Secretariat
Country:	Guyana
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative Description of Project: The general objectives are : To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines To explore the possibilities and identify the requirements and process for establishing a harmonized, pro-public health regional (Caribbean) drug regulation policy (to include generic drugs) and registration system. To identify mechanisms for the development of regional country coalition for joint procurement strategies. Description of Actual Services Provided by Your Staff within the assignment: Development of assessment instrument Desk review, data collection and interviews in countries and qualitative assessment of data. Developing recommendations and strategies for addressing needs and gaps identified at national levels Development of strategies for regional harmonization of drug regulation in CARICOM and the technical requirements for the establishment of a regional platform for future decision-making in drug regulation, Identification of necessity for training programmes and the need for continuing education, Presenting the draft report to the CARICOM Council for Human and Social Development Presenting & discussing draft report and strategic option to the Technical Advisory Group Providing final report
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat
Country:	Dominica
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat
Country:	Dominican Republic
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	Caricom (Caribbean Community Secretariat)
Country:	Barbados
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat)
Country:	Antigua and Barbuda
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat)
Country:	Grenada
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat)
Country:	Guyana
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat)
Country:	Haiti
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat)
Country:	Jamaica
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat)
Country:	St. Lucia
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat)
Country:	Bahamas
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat)
Country:	Belize
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat)
Country:	Montserrat
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat)
Country:	St. Kitts and Nevis
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat)
Country:	St. Vincent and the Grenadines
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat)
Country:	Trinidad & Tobago
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Regional assessment of Patent and Intellectual Property issues and Access to Medicines
Client:	CARICOM (Caribbean Community Secretariat)
Country:	Suriname
Fields of expertise:	Access to Medicine Campaigns, Appraisal, Drug Regulatory Authority Support, National Medicines Policy Development
Description:	Narrative Description of Project: The general objectives of the Assessment were: To explore the possibilities of developing a harmonized, pro-public health regional (Caribbean) IP regulation and drug policy (to include generic drugs) framework To make recommendations on the IP/patent legislation and regulations that will maximize TRIPS flexibilities while being TRIPS compliant To identify the requirements and process for establishing a regional negotiating platform for drugs To identify mechanisms for building/strengthening coalitions and negotiating positions at the WTO, and in bilateral and regional fora for ensuring access to drugs To make recommendations on the adequacy of the systems in Member States for regulation of the pharmaceutical market to ensure the timely supply of safe, effective and quality medicines. Description of Actual Services Provided: Development of a work plan i consultation with the Technical Advisory Group (TAG) and PANCAP Thorough review of all available literature/documents and prior regional studies pertaining to patent legislation, regulations and decrees that focus, in particular, on TRIPS compliance, TRIPS flexibilities; TRIPS + Provisions, and other general issues relating to patent systems; Data collection, analysis of processes and systems that have been adopted in implementing TRIPS flexibilities, TRIPS+ Provisions, at the practical level in the region and provision of a qualitative assessment of the data collected Recommendations and proposal of strategies for addressing needs and gaps identified at national levels and the establishment of a regional platform for future trade negotiations relating to access to medicines and other pharmaceuticals in the context of the Caribbean Single Market and economy. Development of the data collection instrument Test and modification of the data collation instrument in 2 Member States- one that has a well developed IP system and one with a rudimentary system. Trinidad and Tobago and Guyana; Interviews with the relevant persons and agencies at the country and regional level
Year:	2008 - 2009

Assignment:	Medicines Transparency Alliance (MeTA)
Client:	DFID
Country:	Jordan
Fields of expertise:	Access to Medicine Campaigns, Drug Regulatory Authority Support, Drug Supply Management System Strengthening, Essential Drugs Programme Support, Increasing Transparency In Public And Private Pharmaceutical Markets, National Medicines Policy Development, Procurement and Tender Support, Public Private Partnership Interventions, Training and Human Resource Development
Description:	Narrative description of Project: MeTA is a new multi-stakeholder approach for increasing transparency around the selection, procurement, sale and distribution of medicines in Low Income Countries, thereby strengthening governance and encouraging responsible business practices. The MeTA goal is to ensure access to affordable essential drugs in developing countries (MDG 8, target 17). The initiative us being supported financially by DFID during its present Phase One. MeTA brings together, at both the international and national levels, a diverse group of people with an interest in the pharmaceutical sector (stakeholders) to find ways to improve information flows, and increase transparency and accountability about the selection, regulation, procurement, sale, distribution and use of medicines in developing countries. By doing so, MeTA will improve how decisions are made about medicines, improve the way they are purchased and supplied, encourage innovative and responsible business practices, and increase the voice of patients and consumers. Description of actual services provided by your staff within the assignment: The MeTA International Secretariat is tasked to help to support the implementation of MeTA in 7 pilot countries, through facilitating support for the evolution and effective functioning of the National Secretariats, National Multi-Stakeholder Group (NMSGs), and implementation of work plans. Following the establishment of country MeTA structures, the International MeTA Secretariat provides further support to the pilot countries including: Supporting countries to extract and collate data on medicine quality, availability and pricing along the supply chain; Supporting countries to undertake studies assessing the level of transparency and good governance in medicines regulation and procurement; Working with countries to produce country-specific MeTA reports, which would collate data and further analyse and contextualise issues related to medicine quality, availability and price, and to disseminate these reports through the media and public interest groups; as well as exploring policy options and support needed for implementation e.g. of report recommendations. Assist countries in using the data collated through MeTA on medicine policies and regulation as well as quality, availability and prices to try to promote relevant good practice and policy changes to improve access to medicines. HERA contracted staff are responsible for the provision of country specific support under META. Pilot countries are: Ghana, Uganda, Zambia, the Philippines, Jordan, Kyrgyzstan and Peru.
Year:	2008 - 2010

Assignment:	Medicines Transparency Alliance (MeTA)
Client:	DFID
Country:	Ghana
Fields of expertise:	Access to Medicine Campaigns, Drug Pricing Studies, Drug Regulatory Authority Support, Drug Supply Management System Strengthening, Essential Drugs Programme Support, Essential Medicines Financing, Increasing Transparency In Public And Private Pharmaceutical Markets, National Medicines Policy Development, Procurement and Tender Support, Public Private Partnership Interventions, Rational Use Surveys, Training and Human Resource Development
Description:	Narrative description of Project: MeTA is a new multi-stakeholder approach for increasing transparency around the selection, procurement, sale and distribution of medicines in Low Income Countries, thereby strengthening governance and encouraging responsible business practices. The MeTA goal is to ensure access to affordable essential drugs in developing countries (MDG 8, target 17). The initiative us being supported financially by DFID during its present Phase One. MeTA brings together, at both the international and national levels, a diverse group of people with an interest in the pharmaceutical sector (stakeholders) to find ways to improve information flows, and increase transparency and accountability about the selection, regulation, procurement, sale, distribution and use of medicines in developing countries. By doing so, MeTA will improve how decisions are made about medicines, improve the way they are purchased and supplied, encourage innovative and responsible business practices, and increase the voice of patients and consumers. Description of actual services provided by your staff within the assignment: The MeTA International Secretariat is tasked to help to support the implementation of MeTA in 7 pilot countries, through facilitating support for the evolution and effective functioning of the National Secretariats, National Multi-Stakeholder Group (NMSGs), and implementation of work plans. Following the establishment of country MeTA structures, the International MeTA Secretariat provides further support to the pilot countries including: Supporting countries to extract and collate data on medicine quality, availability and pricing along the supply chain; Supporting countries to undertake studies assessing the level of transparency and good governance in medicines regulation and procurement; Working with countries to produce country-specific MeTA reports, which would collate data and further analyse and contextualise issues related to medicine quality, availability and price, and to disseminate these reports through the media and public interest groups; as well as exploring policy options and support needed for implementation e.g. of report recommendations. Assist countries in using the data collated through MeTA on medicine policies and regulation as well as quality, availability and prices to try to promote relevant good practice and policy changes to improve access to medicines. HERA contracted staff are responsible for the provision of country specific support under META. Pilot countries are: Ghana, Uganda, Zambia, the Philippines, Jordan, Kyrgyzstan and Peru.
Year:	2008 - 2010

Assignment:	Medicines Transparency Alliance (MeTA)
Client:	DFID
Country:	Kyrgyzstan
Fields of expertise:	Access to Medicine Campaigns, Drug Pricing Studies, Drug Regulatory Authority Support, Drug Supply Management System Strengthening, Essential Drugs Programme Support, Essential Medicines Financing, Increasing Transparency In Public And Private Pharmaceutical Markets, National Medicines Policy Development, Public Private Partnership Interventions, Rational Use Surveys, Training and Human Resource Development
Description:	Narrative description of Project: MeTA is a new multi-stakeholder approach for increasing transparency around the selection, procurement, sale and distribution of medicines in Low Income Countries, thereby strengthening governance and encouraging responsible business practices. The MeTA goal is to ensure access to affordable essential drugs in developing countries (MDG 8, target 17). The initiative us being supported financially by DFID during its present Phase One. MeTA brings together, at both the international and national levels, a diverse group of people with an interest in the pharmaceutical sector (stakeholders) to find ways to improve information flows, and increase transparency and accountability about the selection, regulation, procurement, sale, distribution and use of medicines in developing countries. By doing so, MeTA will improve how decisions are made about medicines, improve the way they are purchased and supplied, encourage innovative and responsible business practices, and increase the voice of patients and consumers. Description of actual services provided by your staff within the assignment: The MeTA International Secretariat is tasked to help to support the implementation of MeTA in 7 pilot countries, through facilitating support for the evolution and effective functioning of the National Secretariats, National Multi-Stakeholder Group (NMSGs), and implementation of work plans. Following the establishment of country MeTA structures, the International MeTA Secretariat provides further support to the pilot countries including: Supporting countries to extract and collate data on medicine quality, availability and pricing along the supply chain; Supporting countries to undertake studies assessing the level of transparency and good governance in medicines regulation and procurement; Working with countries to produce country-specific MeTA reports, which would collate data and further analyse and contextualise issues related to medicine quality, availability and price, and to disseminate these reports through the media and public interest groups; as well as exploring policy options and support needed for implementation e.g. of report recommendations. Assist countries in using the data collated through MeTA on medicine policies and regulation as well as quality, availability and prices to try to promote relevant good practice and policy changes to improve access to medicines. HERA contracted staff are responsible for the provision of country specific support under META. Pilot countries are: Ghana, Uganda, Zambia, the Philippines, Jordan, Kyrgyzstan and Peru.
Year:	2008 - 2010

Assignment:	Medicines Transparency Alliance (MeTA)
Client:	DFID
Country:	Peru
Fields of expertise:	Access to Medicine Campaigns, Drug Pricing Studies, Drug Regulatory Authority Support, Drug Supply Management System Strengthening, Essential Drugs Programme Support, Essential Medicines Financing, Increasing Transparency In Public And Private Pharmaceutical Markets, National Medicines Policy Development, Public Private Partnership Interventions, Rational Use Surveys, Training and Human Resource Development
Description:	Narrative description of Project: MeTA is a new multi-stakeholder approach for increasing transparency around the selection, procurement, sale and distribution of medicines in Low Income Countries, thereby strengthening governance and encouraging responsible business practices. The MeTA goal is to ensure access to affordable essential drugs in developing countries (MDG 8, target 17). The initiative us being supported financially by DFID during its present Phase One. MeTA brings together, at both the international and national levels, a diverse group of people with an interest in the pharmaceutical sector (stakeholders) to find ways to improve information flows, and increase transparency and accountability about the selection, regulation, procurement, sale, distribution and use of medicines in developing countries. By doing so, MeTA will improve how decisions are made about medicines, improve the way they are purchased and supplied, encourage innovative and responsible business practices, and increase the voice of patients and consumers. Description of actual services provided by your staff within the assignment: The MeTA International Secretariat is tasked to help to support the implementation of MeTA in 7 pilot countries, through facilitating support for the evolution and effective functioning of the National Secretariats, National Multi-Stakeholder Group (NMSGs), and implementation of work plans. Following the establishment of country MeTA structures, the International MeTA Secretariat provides further support to the pilot countries including: Supporting countries to extract and collate data on medicine quality, availability and pricing along the supply chain; Supporting countries to undertake studies assessing the level of transparency and good governance in medicines regulation and procurement; Working with countries to produce country-specific MeTA reports, which would collate data and further analyse and contextualise issues related to medicine quality, availability and price, and to disseminate these reports through the media and public interest groups; as well as exploring policy options and support needed for implementation e.g. of report recommendations. Assist countries in using the data collated through MeTA on medicine policies and regulation as well as quality, availability and prices to try to promote relevant good practice and policy changes to improve access to medicines. HERA contracted staff are responsible for the provision of country specific support under META. Pilot countries are: Ghana, Uganda, Zambia, the Philippines, Jordan, Kyrgyzstan and Peru.
Year:	2008 - 2010

Assignment:	Medicines Transparency Alliance (MeTA)
Client:	DFID
Country:	The Philippines
Fields of expertise:	Access to Medicine Campaigns, Drug Pricing Studies, Drug Regulatory Authority Support, Drug Supply Management System Strengthening, Essential Drugs Programme Support, Essential Medicines Financing, Increasing Transparency In Public And Private Pharmaceutical Markets, National Medicines Policy Development, Public Private Partnership Interventions, Rational Use Surveys, Training and Human Resource Development
Description:	Narrative description of Project: MeTA is a new multi-stakeholder approach for increasing transparency around the selection, procurement, sale and distribution of medicines in Low Income Countries, thereby strengthening governance and encouraging responsible business practices. The MeTA goal is to ensure access to affordable essential drugs in developing countries (MDG 8, target 17). The initiative us being supported financially by DFID during its present Phase One. MeTA brings together, at both the international and national levels, a diverse group of people with an interest in the pharmaceutical sector (stakeholders) to find ways to improve information flows, and increase transparency and accountability about the selection, regulation, procurement, sale, distribution and use of medicines in developing countries. By doing so, MeTA will improve how decisions are made about medicines, improve the way they are purchased and supplied, encourage innovative and responsible business practices, and increase the voice of patients and consumers. Description of actual services provided by your staff within the assignment: The MeTA International Secretariat is tasked to help to support the implementation of MeTA in 7 pilot countries, through facilitating support for the evolution and effective functioning of the National Secretariats, National Multi-Stakeholder Group (NMSGs), and implementation of work plans. Following the establishment of country MeTA structures, the International MeTA Secretariat provides further support to the pilot countries including: Supporting countries to extract and collate data on medicine quality, availability and pricing along the supply chain; Supporting countries to undertake studies assessing the level of transparency and good governance in medicines regulation and procurement; Working with countries to produce country-specific MeTA reports, which would collate data and further analyse and contextualise issues related to medicine quality, availability and price, and to disseminate these reports through the media and public interest groups; as well as exploring policy options and support needed for implementation e.g. of report recommendations. Assist countries in using the data collated through MeTA on medicine policies and regulation as well as quality, availability and prices to try to promote relevant good practice and policy changes to improve access to medicines. HERA contracted staff are responsible for the provision of country specific support under META. Pilot countries are: Ghana, Uganda, Zambia, the Philippines, Jordan, Kyrgyzstan and Peru.
Year:	2008 - 2010

Assignment:	Medicines Transparency Alliance (MeTA)
Client:	DFID
Country:	Uganda
Fields of expertise:	Access to Medicine Campaigns, Drug Pricing Studies, Drug Regulatory Authority Support, Drug Supply Management System Strengthening, Essential Drugs Programme Support, Essential Medicines Financing, Increasing Transparency In Public And Private Pharmaceutical Markets, National Medicines Policy Development, Public Private Partnership Interventions, Rational Use Surveys, Training and Human Resource Development
Description:	Narrative description of Project: MeTA is a new multi-stakeholder approach for increasing transparency around the selection, procurement, sale and distribution of medicines in Low Income Countries, thereby strengthening governance and encouraging responsible business practices. The MeTA goal is to ensure access to affordable essential drugs in developing countries (MDG 8, target 17). The initiative us being supported financially by DFID during its present Phase One. MeTA brings together, at both the international and national levels, a diverse group of people with an interest in the pharmaceutical sector (stakeholders) to find ways to improve information flows, and increase transparency and accountability about the selection, regulation, procurement, sale, distribution and use of medicines in developing countries. By doing so, MeTA will improve how decisions are made about medicines, improve the way they are purchased and supplied, encourage innovative and responsible business practices, and increase the voice of patients and consumers. Description of actual services provided by your staff within the assignment: The MeTA International Secretariat is tasked to help to support the implementation of MeTA in 7 pilot countries, through facilitating support for the evolution and effective functioning of the National Secretariats, National Multi-Stakeholder Group (NMSGs), and implementation of work plans. Following the establishment of country MeTA structures, the International MeTA Secretariat provides further support to the pilot countries including: Supporting countries to extract and collate data on medicine quality, availability and pricing along the supply chain; Supporting countries to undertake studies assessing the level of transparency and good governance in medicines regulation and procurement; Working with countries to produce country-specific MeTA reports, which would collate data and further analyse and contextualise issues related to medicine quality, availability and price, and to disseminate these reports through the media and public interest groups; as well as exploring policy options and support needed for implementation e.g. of report recommendations. Assist countries in using the data collated through MeTA on medicine policies and regulation as well as quality, availability and prices to try to promote relevant good practice and policy changes to improve access to medicines. HERA contracted staff are responsible for the provision of country specific support under META. Pilot countries are: Ghana, Uganda, Zambia, the Philippines, Jordan, Kyrgyzstan and Peru.
Year:	2008 - 2010

Assignment:	Medicines Transparency Alliance (MeTA)
Client:	DFID
Country:	Zambia
Fields of expertise:	Access to Medicine Campaigns, Drug Pricing Studies, Drug Regulatory Authority Support, Drug Supply Management System Strengthening, Essential Drugs Programme Support, Essential Medicines Financing, Increasing Transparency In Public And Private Pharmaceutical Markets, National Medicines Policy Development, Public Private Partnership Interventions, Rational Use Surveys, Training and Human Resource Development
Description:	Narrative description of Project: MeTA is a new multi-stakeholder approach for increasing transparency around the selection, procurement, sale and distribution of medicines in Low Income Countries, thereby strengthening governance and encouraging responsible business practices. The MeTA goal is to ensure access to affordable essential drugs in developing countries (MDG 8, target 17). The initiative us being supported financially by DFID during its present Phase One. MeTA brings together, at both the international and national levels, a diverse group of people with an interest in the pharmaceutical sector (stakeholders) to find ways to improve information flows, and increase transparency and accountability about the selection, regulation, procurement, sale, distribution and use of medicines in developing countries. By doing so, MeTA will improve how decisions are made about medicines, improve the way they are purchased and supplied, encourage innovative and responsible business practices, and increase the voice of patients and consumers. Description of actual services provided by your staff within the assignment: The MeTA International Secretariat is tasked to help to support the implementation of MeTA in 7 pilot countries, through facilitating support for the evolution and effective functioning of the National Secretariats, National Multi-Stakeholder Group (NMSGs), and implementation of work plans. Following the establishment of country MeTA structures, the International MeTA Secretariat provides further support to the pilot countries including: Supporting countries to extract and collate data on medicine quality, availability and pricing along the supply chain; Supporting countries to undertake studies assessing the level of transparency and good governance in medicines regulation and procurement; Working with countries to produce country-specific MeTA reports, which would collate data and further analyse and contextualise issues related to medicine quality, availability and price, and to disseminate these reports through the media and public interest groups; as well as exploring policy options and support needed for implementation e.g. of report recommendations. Assist countries in using the data collated through MeTA on medicine policies and regulation as well as quality, availability and prices to try to promote relevant good practice and policy changes to improve access to medicines. HERA contracted staff are responsible for the provision of country specific support under META. Pilot countries are: Ghana, Uganda, Zambia, the Philippines, Jordan, Kyrgyzstan and Peru.
Year:	2008 - 2010

Assignment:	Mid-term Review of EC/ACP/WHO Partnership on Pharmaceutical Policies
Client:	EC - AIDCO
Country:	Global
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Essential Medicines Financing, Monitoring and Evaluation, National Medicines Policy Development
Description:	Narrative Description of Project: Study of the achievements of the programme, its contribution to the overall objective, and performance in terms of programme purpose and results. Estimation of the quality of work planning, budgeting and risk management. Analysis of constraints and proposal of solutions. Analysis of the degree of coherence of the programme with the country national drugs plans at governmental level and activities undertaken by the relevant stakeholders,. Analysis of the degree of coordination and complementarities of project’s activities with other donor’s activities at country and global levels. Analysis of the degree of sustainability of project benefits Analysis of the degree of respect of EU visibility and publicity in WHO implementation approach. Proposal of measures and recommendations for change to project scope in order to support effective implementation. Description of Actual Services Provided: Briefing in Brussels with EU services AIDCO/C/4 Desk-audits and interviews at WHO Offices in Geneva Visits to regional offices: Brazzaville and Manila Country visits to Nigeria and Tanzania: contacts with officials at the EC Delegations, and the key donors in pharmaceutical and essential medicine area and field visits. Draft report summarizing findings and recommendations Validation workshop in Brussels Submission Final Report
Year:	2006

Assignment:	Mid-term Review of EC/ACP/WHO Partnership on Pharmaceutical Policies
Client:	EC - AIDCO
Country:	Nigeria
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Essential Medicines Financing, Monitoring and Evaluation, National Medicines Policy Development
Description:	Narrative Description of Project: Study of the achievements of the programme, its contribution to the overall objective, and performance in terms of programme purpose and results. Estimation of the quality of work planning, budgeting and risk management. Analysis of constraints and proposal of solutions. Analysis of the degree of coherence of the programme with the country national drugs plans at governmental level and activities undertaken by the relevant stakeholders,. Analysis of the degree of coordination and complementarities of project’s activities with other donor’s activities at country and global levels. Analysis of the degree of sustainability of project benefits Analysis of the degree of respect of EU visibility and publicity in WHO implementation approach. Proposal of measures and recommendations for change to project scope in order to support effective implementation. Description of Actual Services Provided: Briefing in Brussels with EU services AIDCO/C/4 Desk-audits and interviews at WHO Offices in Geneva Visits to regional offices: Brazzaville and Manila Country visits to Nigeria and Tanzania: contacts with officials at the EC Delegations, and the key donors in pharmaceutical and essential medicine area and field visits. Draft report summarizing findings and recommendations Validation workshop in Brussels Submission Final Report
Year:	2006

Assignment:	Mid-term Review of EC/ACP/WHO Partnership on Pharmaceutical Policies
Client:	EC - AIDCO
Country:	Tanzania / Zanzibar
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Essential Medicines Financing, Monitoring and Evaluation, National Medicines Policy Development
Description:	Narrative Description of Project: Study of the achievements of the programme, its contribution to the overall objective, and performance in terms of programme purpose and results. Estimation of the quality of work planning, budgeting and risk management. Analysis of constraints and proposal of solutions. Analysis of the degree of coherence of the programme with the country national drugs plans at governmental level and activities undertaken by the relevant stakeholders,. Analysis of the degree of coordination and complementarities of project’s activities with other donor’s activities at country and global levels. Analysis of the degree of sustainability of project benefits Analysis of the degree of respect of EU visibility and publicity in WHO implementation approach. Proposal of measures and recommendations for change to project scope in order to support effective implementation. Description of Actual Services Provided: Briefing in Brussels with EU services AIDCO/C/4 Desk-audits and interviews at WHO Offices in Geneva Visits to regional offices: Brazzaville and Manila Country visits to Nigeria and Tanzania: contacts with officials at the EC Delegations, and the key donors in pharmaceutical and essential medicine area and field visits. Draft report summarizing findings and recommendations Validation workshop in Brussels Submission Final Report
Year:	2006

Assignment:	Mid-term Review of EC/ACP/WHO Partnership on Pharmaceutical Policies
Client:	EC - AIDCO
Country:	Congo Brazzaville
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Essential Medicines Financing, Monitoring and Evaluation, National Medicines Policy Development
Description:	Narrative Description of Project: Study of the achievements of the programme, its contribution to the overall objective, and performance in terms of programme purpose and results. Estimation of the quality of work planning, budgeting and risk management. Analysis of constraints and proposal of solutions. Analysis of the degree of coherence of the programme with the country national drugs plans at governmental level and activities undertaken by the relevant stakeholders,. Analysis of the degree of coordination and complementarities of project’s activities with other donor’s activities at country and global levels. Analysis of the degree of sustainability of project benefits Analysis of the degree of respect of EU visibility and publicity in WHO implementation approach. Proposal of measures and recommendations for change to project scope in order to support effective implementation. Description of Actual Services Provided: Briefing in Brussels with EU services AIDCO/C/4 Desk-audits and interviews at WHO Offices in Geneva Visits to regional offices: Brazzaville and Manila Country visits to Nigeria and Tanzania: contacts with officials at the EC Delegations, and the key donors in pharmaceutical and essential medicine area and field visits. Draft report summarizing findings and recommendations Validation workshop in Brussels Submission Final Report
Year:	2006

Assignment:	Mid-term Review of EC/ACP/WHO Partnership on Pharmaceutical Policies
Client:	EC - AIDCO
Country:	The Philippines
Fields of expertise:	Drug Regulatory Authority Support, Essential Drugs Programme Support, Essential Medicines Financing, Monitoring and Evaluation, National Medicines Policy Development
Description:	Narrative Description of Project: Study of the achievements of the programme, its contribution to the overall objective, and performance in terms of programme purpose and results. Estimation of the quality of work planning, budgeting and risk management. Analysis of constraints and proposal of solutions. Analysis of the degree of coherence of the programme with the country national drugs plans at governmental level and activities undertaken by the relevant stakeholders,. Analysis of the degree of coordination and complementarities of project’s activities with other donor’s activities at country and global levels. Analysis of the degree of sustainability of project benefits Analysis of the degree of respect of EU visibility and publicity in WHO implementation approach. Proposal of measures and recommendations for change to project scope in order to support effective implementation. Description of Actual Services Provided: Briefing in Brussels with EU services AIDCO/C/4 Desk-audits and interviews at WHO Offices in Geneva Visits to regional offices: Brazzaville and Manila Country visits to Nigeria and Tanzania: contacts with officials at the EC Delegations, and the key donors in pharmaceutical and essential medicine area and field visits. Draft report summarizing findings and recommendations Validation workshop in Brussels Submission Final Report
Year:	2006

Assignment:	Diagnosis and reorganisation of the pharmaceutical sector
Client:	World Bank
Country:	Rwanda
Fields of expertise:	Drug Regulatory Authority Support, Drug Supply Management System Strengthening, Essential Drugs Programme Support, Essential Medicines Financing, Health Sector Reform, Medical Store Evaluation, National Medicines Policy Development, Pharmaceutical Sector Review, Planning, Organisation and Management, Quantification of Essential Drug Needs, Rational Use Surveys, Selection of Essential Medicines, Training and Human Resource Development
Description:	Narrative Description of Project: Diagnosis and reorganisation of the pharmaceutical sector in Rwanda (public and private sector). Development of a national policy and legislation for the pharmaceutical sector. Institutional strengthening of the Pharmaceutical Department of the Ministry of Health. Technical and organisational proposals for a new structure for a national central medical store. Quantification of the national needs for essential drugs. Development of the strategies for procurement, supply, storing and distribution of the essential drugs. Proposal for a diagnostic and treatment standard. Strategies for the registration, quality control and rational use of drugs. Development of financial policies for drugs (custom duties, price regulation, etc.). Proposal for the financing of the development plan of the pharmaceutical sector. Description of Actual Services Provided: Responsible for a detailed analysis of the pharmaceutical sector, including policy, legislation, provision and supply of drugs, drug needs by level and by sector, drug use, drug registration, drug financing aspects. Provided assistance to the Ministry of Health in all the above fields to develop proposals to reform. Assisted the Ministry of Health in developing a new central medical stores structure as a parastatal organisation. Developed a financial plan for all proposed reforms. Consensus development at a national and international workshop where proposals for reform have been presented. The actual and functional national central medical store in Kigali is based on the feasibility study and the technical proposals made by HERA-CDP.
Year:	1993 - 1994

Assignment:	Review of the Pharmaceutical Sector
Client:	World Bank - Ministry of Health
Country:	Kenya
Fields of expertise:	Drug Regulatory Authority Support, Drug Supply Management System Strengthening, Essential Drugs Programme Support, Health Policy and Policy Dialogue, Health Sector Reform, Health Sector Review or Health Sector Diagnosis, Monitoring and Evaluation, National Medicines Policy Development, Pharmaceutical Sector Review, Procurement and Tender Support, Quantification of Essential Drug Needs, Rational Use Surveys
Description:	Narrative description of Project: The Government of Kenya, with support from its partners including the World Bank, has committed itself to a series of reform efforts in the health sector. As part of this , the MOH commissioned a comprehensive review of the pharmaceutical sector. The review was contracted in 4 different consultancies of which HERA completed 3 parts: Consultancy for Evaluation of Pharmaceutical Access in Kenya, including an Institutional Capacity Assessment of the MOH and KEMSA Consultancy for Evaluating/Improving Quality Assurance and Sustainability in the Medical Supplies Sub-sector in Kenya Consultancy to strengthen the logistics Management and the Rational Use of Drugs in Kenya. Description of actual services provided: Evaluation of Pharmaceutical Access in Kenya: Description of geographical, physical and financial access to drugs in Kenya, particularly for the diseases of poverty, in both public and private sectors; Evaluation of the structure, functioning and outcomes of the existing drug supply systems (including the procurement, warehousing and distribution of drugs to all levels of the health care system); Assessment of the structure, functioning and outcomes of the existing pharmaceutical financing and pricing systems from an efficiency and equity perspective; Development of alternative proposals for efficient and equitable systems of drug supply management, financing and pricing. Evaluating/ Improving Quality Assurance and Sustainability in the Medical Supplies Sub-sector : Description and evaluation of the overall structure, process and performance of drug quality assurance/control systems at both central and provincial levels; Assessment of the procedures ensuring the quality of drugs and of manufacturing facilities, the thoroughness and frequency of these quality inspections and the overall effectiveness of the quality assurance/control systems; Detailed analysis of all the sources and uses of Drug Control Authority Funds; Development of recommendations to ensure that the systems for drug quality assurance at all levels of the health system in the public and private sectors function efficiently and effectively in the future. Strengthening the Logistics Management and Rational Use of Drugs: Description and analysis of the existing patterns of drug prescription, dispensing and consumption in the public and private sectors. Review of the logistics management system in the public and private sectors and recommendations for strengthening and developing a national procurement and logistics management action plan; Evaluation of the existing policies, norms, standards and practices related to the use of pharmaceuticals by health professionals and consumers; Development of alternative proposals for the establishment of an effective program for rational drug use (including an essential drugs policy and generics strategy).
Year:	2004 - 2005