EMA public consultation

EMA published for public consultation a guideline on quality, non-clinical and clinical aspects of medicines containing genetically modified cell.

November 20, 2018

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Share your ideas by using the template linked in the guideline until 31 July 2019.

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Brexit updates for human use medicinal products approved via MRP/DCP

December 21, 2020

As Brexit is quickly coming closer, the CMDh has published an updated version of the Practical guidance for procedures related to Brexit for medicinal products for human use approved via MRP/DCP in December 2020.

Javier Febrero Alija – New Regulatory Information Manager

December 17, 2020

Asphalion is excited and proud to officially welcome Javier Febrero Alija to its team as Regulatory Information Manager, expert in Data Management and RIMS.

Season’s Greetings

December 17, 2020

We wish you Happy ‘Xmas, Prosperous New Year and Health for you and your loved ones.

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EMA public consultation

EMA published for public consultation a guideline on quality, non-clinical and clinical aspects of medicines containing genetically modified cell.

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Related news and events

Brexit updates for human use medicinal products approved via MRP/DCP

Javier Febrero Alija – New Regulatory Information Manager

Season’s Greetings

About

Team

Partners

CSR

Careers

EMA public consultation

EMA published for public consultation a guideline on quality, non-clinical and clinical aspects of medicines containing genetically modified cell.

Search

Filter by category

Related news and events

Brexit updates for human use medicinal products approved via MRP/DCP

Javier Febrero Alija – New Regulatory Information Manager

Season’s Greetings

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