The European Medicines Agency (EMEA) hosted an information day at its London, UK, offices, in conjunction with the Brussels, Belgium-based European Federation of Pharmaceutical Industries and Associations on February 5.
The one-day event assembled representatives from the EMEA, the drug industry and a select media presence. The general areas covered by the conference were: analysis of the performance indicators for both organizations in 2006 for Initial Marketing Authorization Applications and for type II Variation Applications (Extension of Indications); a review of the first year's experience of new drug legislation (Conditional Marketing Authorizations and Risk Management Plans); implementation of the new pediatric medicines regulation; and the Innovative Medicines Initiative.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
| Headless Content Management with Blaze