The Playbook provides a practical, user-friendly guide to navigating the complexities of data sharing in IMI/IHI collaborative health research projects, outlining key concepts, roles, decision points, common challenges, and strategies to address legal, technical, and organisational obstacles. It encourages early planning, stakeholder engagement, and adoption of standardised best practices to accelerate data sharing and improve research efficiency across multi-partner consortia

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TTO Guidance and assessment model for Socially Responsible Licensing and Negotiation

Published by FAST (Centre for Future Affordable & Sustainable Therapy Development)

LicensingNegociationTTO

This guide is designed to assist Public Research Organizations (PROs), including universities and university medical centers, in enhancing the potential for their scientific discoveries to benefit society through commercialization (valorization). To achieve this, it is essential to convert research findings into practical applications (innovation). Typically, this is facilitated by private entities that utilize intellectual property (IP) licensed from PROs. The purpose of this guide is to simplify this challenging process.”

The corrected version resolves typos and uses clearer language to improve readability and professional tone

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When you plan in reverse, you start with your end goal and then work your way backwards from there to develop a plan of action. Working backwards in this way can give you a much clearer picture of what and how much must be accomplished during each phase of a project. It can also help you identify and avoid unnecessary activities

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A target product profile (TPP) outlines the desired characteristics of a new drug or other medical intervention (e.g diagnostic tool). TPPs describe intended use, target populations and other desired attributes of products, including safety and efficacy-related characteristics. In industry TPPs are used as planning tools that guide development towards desired characteristics. In the regulatory context, TPPs are considered as tools to frame development in relation to submission of product dossiers.

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CORBEL is an initiative of thirteen new biological and medical research infrastructures (BMS RIs), which together will create a platform for harmonised user access to biological and medical technologies, biological samples and data services required by cutting-edge biomedical research. CORBEL will boost the efficiency, productivity and impact of European biomedical research

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