The US Association for Accessible Medicines’ (AAM) Biosimilars Council has released an update on major developments in the biosimilars sector by executive director Craig Burten.
In the month of June, both chambers of Congress made progress in advancing legislation to reauthorize the Biosimilar User Fee Act (BsUFA), with the House of Representatives passing its bill, and the Senate HELP Committee approving its version for the full Senate’s consideration.
This legislation is critical to the future of patient access to biosimilars and provides the US Food and Drug Administration (FDA) with the resources it needs to review new biosimilar products.
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