This document is part of the MRC’s Ethics Series and sets out the MRC’s expectations for MRC Units and Institutes and MRC grant holders with respect to the use of human biological samples in research.
This brochure provides a detailed layman’s overview of the drug R&D process, which may be particularly useful to TT professionals without a pharmaceutical research background.
This OECD recommendation provides guidelines for the establishment, management, governance, operation, access, use and discontinuation of Human Biobanks and Genetic Research Databases.
This document presents the guidelines for entering into research agreements with private companies, which have been adopted by the Danish teaching hospitals.
Drug Discovery and Development Centres affiliated with or integrated in academic institutes have created an association to exchange knowledge and expertise in translating health research into new medicines.
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