The US Food and Drug Administration has approved its lowest number of new products since 1983, according to Ira Loss, executive vice president of specialist financial firm Washington Analysis. The news, which was not immediately confirmed by the federal agency, has stirred a debate between drugmakers and the FDA over the cause for the drop in successful drug reviews.
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