Workshops for micro, small and medium-sized enterprises: focus on non-clinical aspects

Date: 03/10/2016
Location: European Medicines Agency, London, UK
This workshop aims to provide an overview of non-clinical data requirements for the authorisation of human medicinal products, how to address these during the medicinal product development, and detail the approaches for biological and advanced therapy medicinal products. A regulatory brief on the new PRIME scheme is also included in the programme.

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