The US Food and Drug Administration has authorized emergency use of a novel diagnostic test for COVID-19, from Swiss pharma giant Roche (ROG: SIX).
The cobas SARS-CoV-2 Test was granted an Emergency Use Authorization (EUA) just a day after the firm applied.
Commentators have criticized US President Donald Trump for offering mixed and sometimes contradictory messages to the public, and for failing to prepare adequately. A lack of suitable tests has been of chief concern to lawmakers in the country.
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
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze