EMA updates on fee reduction for SMEs developing orphan drugs in 2013

19 December 2012

The European Medicines Agency’s policy on fee reductions for orphan medicinal products is set to continue into 2013. The policy, as advised by the Agency’s Committee for Orphan Medicinal Products (COMP), focuses primarily on assistance to micro, small and medium-sized enterprises (SMEs) with the objective of providing incentives to support research and innovation for medicines intended for the diagnosis, prevention or treatment of rare diseases.

Fee reductions for SMEs

The following services will remain free-of-charge for SMEs in 2013:

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





Today's issue

Company Spotlight





More Features in Biotechnology