FDA's CDER points out progress from last year

8 January 2019
janet_woodcock_large-1-

The start of 2019 has not been easy for the US Food and Drug Administration (FDA), but the agency and its Center for Drug Evaluation and Research (CDER) can reflect on a pretty successful 2018.

And that is exactly what Janet Woodcock (pictured above), director of the CDER, has done in a review of the year, including looking back at some of the most important FDA approvals.

She wrote in a column that the year had been important for patients with rare diseases.

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 Pharmaceutical