Mandate

• Develop a questionnaire allowing collection of essential information on research centres/organisations¹. The information gathered through the questionnaire should allow at a later stage complex searches of the inventory by terms such as location (country), expertise, main field of research, but also outcome-related terms like ADRs, drug-drug-interaction etc
• Identify additional existing EU PhEpi and PhV research resources; define exclusion/inclusion criteria for participating centres/organisations, e.g. source of funding, size of CROs, etc.
• Develop an electronic inventory: identify needs and deliverables of such a tool; liaise with the European Medicines Agency IT project manager
• Input to the design of the European Medicines Agency web page

(¹ E.g. academic centres or other clinical research organisations, as well as existing EU networks)