The FDA: 2021 activities at a glance

fda-blog-700

By Dr Nicola Davies

The year 2021 saw the US Food and Drug Administration approval of 46 novel drugs,1 80 first generics,2 two biosimilars,3 and nine novel biologics,4 as of December 10, 2021. In addition to the regulatory approval of therapeutics, the FDA has been addressing many other pressing public health concerns. We take a brief look at some of the FDA’s activities this year.

Management of the COVID-19 pandemic

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