Ireland-incorporated rare diseases giant Shire (LSE: SHP) announced on Friday that it had receieved approval from the US Food and Drug Administration (FDA) on its first submission for a new plasma manufacturing center in the state of Georgia.
The facility, which has received approval for the manufacture of Gammagard (immunoglobulin 10%), would add 30% to the company's plasma production capacity when completed. The value of Shire's plasma portfolio has increased 18% in 2017 and a further 12% in Q1 of 2018.
"The site will support Shire’s growing immunology franchise"
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