US FDA looks to promote development of coronavirus diagnostics and treatments

28 January 2020
fda_big

As the general public and drugmakers alike scramble to find out more information about the emerging coronavirus outbreak in Wuhan, China, the US regulator has provided an update on critical actions to advance medical countermeasures.

The US Food and Drug Administration said it would collaborate with interagency partners, developers and other regulators to expedite the development and availability of medical products.

The FDA is looking to help promote the development of products which are needed to diagnose, treat, mitigate and prevent outbreaks such as the coronavirus.

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