Drug Development & Regulatory Affairs

The Scientific, Regulatory, Manufacturing (SRM) team at EFPIA supports a lot of specialised experts groups, e.g. Clinical Development Expert Group, Technical Development Expert Group, Pharmacovigilance Expert Group and others. These committees draft EFPIA position papers which then are agreed by the EFPIA Secretariat. Several of these position papers are published here. 

The SRM team also administers a lot of  EFPIA responses to mainly the Commission and the European Medicines Agency EMA. You will also find below all these EFPIA responses submitted from May 2014.

EMA / EC CONSULTATIONS

2016

2015

2014

POSITION PAPERS

PUBLICATIONS