Earma Annual Conference 23 june 2011 - Magali Poinot (parts 2&3)
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The document summarizes how the Innovative Medicines Initiative (IMI) supports collaborative research projects. IMI provides funding from the EU and contributions from pharmaceutical companies. Projects involve a range of participants, including academia, small businesses, patient groups, and regulators. The document outlines IMI's rules around funding, intellectual property, and participation requirements.
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Earma Annual Conference 23 june 2011 - Magali Poinot (parts 2&3)
- 1. The writing and implementation of the Innovative Medicines Initiative projects Part II Magali Poinot IMI Legal Manager www. imi .europa. eu
- 7. Overall structure of IMI projects EFPIA comp EFPIA comp EFPIA comp EFPIA comp Academic Academic Regulators SME SME Patient Org. IMI beneficiaries (eligible for public funding) EFPIA ‘in kind’ contribution EFPIA comp EFPIA comp “ Applicants consortium” “ EFPIA consortium” (no public funding)
- 17. One policy, multiple interests Freedom of Access Dissemination of information Compensation for IP Support for EU Industry Incentive to participate Innovative Medicines Research Use for project participants Fair and reasonable terms for others Data in public domain within a year Only necessary background included Compensation within fair and reasonable terms Direct exploitation rights (academia/SME) Terms known at outset (Pharma) Terms accommodate a the needs of a spectrum of interests - large and small
- 22. Useful definitions (1/2) Start of End of the project the project Implementation Background Foreground // Sideground // ( generated under the Project but outside the Project Objectives and not needed for implementation or Research Use ) possible access rights
- 28. Access Rights (2/2) N.A. Fair & reasonable terms as determined in Project Agreement Fair & reasonable terms for Background needed for using Foreground as determined in Project Agreement Third Parties for Research Use after the Project N.A. To be negotiated To be negotiated Participants and affiliates or Third Parties for Direct Exploitation N.A. Royalty-free OR Fair & reasonable terms as determined in Project Agreement Royalty-free OR Fair & reasonable terms for Background needed for using Foreground as determined in Project Agreement Participants and affiliates for Research Use N.A. Royalty-free Royalty-free Participants for completion of the Project Sideground Foreground Background (necessary and identified) Access rights granted by a Participant to/on
- 32. The writing and implementation of the Innovative Medicines Initiative projects Part III www. imi .europa. eu