In advance of today's US Federal Trade Commission workshop on follow-on biologics, or biosimilars, health advocacy organizations from across the country jointly submitted a letter to FTC Commissioner Edith Ramirez, urging her to give patient safety and consumer protection the important weight and priority they deserve.
The Alliance for Patient Access (AfPA) and 14 other organizations encouraged the FTC to support the adoption of distinguishable names for all biologic products, including biosimilars.
The letter applauded the FTC's decision to hold hearings to examine issues of market access and competition for products that will be approved by the Food and Drug Administration through this new pathway. It said that biosimilars can be of value to patients only if they are accessible and affordable. However, there is a third focus that is as important as the other two, namely patient safety and consumer protection.
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