<--- Back to Details
First PageDocument Content
Pharmaceuticals policy / Medicine / Research / EudraVigilance / Pharmaceutical industry / Pharmacology / European Medicines Agency / Pharmacovigilance / Electronic data interchange / Clinical research / Health / Drug safety
Date: 2015-01-21 09:57:46
Pharmaceuticals policy
Medicine
Research
EudraVigilance
Pharmaceutical industry
Pharmacology
European Medicines Agency
Pharmacovigilance
Electronic data interchange
Clinical research
Health
Drug safety

EU ICSR Implementation Guide

Add to Reading List

Source URL: www.ema.europa.eu

Download Document from Source Website

File Size: 837,81 KB

Share Document on Facebook

Similar Documents

The European Agency for the Evaluation of Medicinal Products Veterinary Medicines and Inspections EMEA/CVMPFINAL COMMITTEE FOR VETERINARY MEDICINAL PRODUCTS

DocID: 1vrLd - View Document

7 May 2018 EMAHuman Medicines Research and Development Support Division European Medicines Agency Guidance for applicants seeking access to PRIME scheme

DocID: 1vlIp - View Document

The European Agency for the Evaluation of Medicinal Products Evaluation of Medicines for Human Use London, 23 January 2003 CPMP/SWP

DocID: 1ucvu - View Document

2 March 2016 EMAExternal guidance on the implementation of the European Medicines Agency policy on the publication of clinical data for medicinal products for human use

DocID: 1sVev - View Document

European Medicines Agency: Celebrating 20 years

DocID: 1sUY9 - View Document