
European vaccine policy led a relatively quiet week for global medicines regulation, with the European Medicines Agency recommending that COVID-19 vaccines be updated to target the XFG variant for the 2026/2027 vaccination campaign.
The US Food and Drug Administration added several drug guidance and data updates, while Japan’s Pharmaceuticals and Medical Devices Agency posted new review and safety materials. India’s Central Drugs Standard Control Organisation also recorded fresh clinical trial approvals, including multinational sponsor activity.
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
| Headless Content Management with Blaze