EC, EMEA and FDA confirm their commitment to cooperation on advancing medicines

19 October 2008

The European Commission, the European Medicines Agency (EMEA) and the US Food and Drug Administration have affirmed their commitment to regulatory cooperation and to intensifying their interactions in several new areas.

Meeting in the UK for the annual review of cooperative activities undertaken under the scope of their confidentiality arrangements, the European Union and US authorities agreed to expand collaboration in the areas of advanced-therapy medicines and nanotechnology-derived medicinal products, as well as on the exchange of pharmacovigilance information.

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 account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
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









Company Spotlight