Experts at the MHRA have begun to post their experiences and insights into MAA and CTA submissions, with the aim of keeping regulatory professionals well-informed.
The blog, released in January 2017, will be regularly updated with posts from experts in all aspects of the medicinal product life cycle with information to prevent common submission pitfalls. So far, posts on Type 1B variations and the MHRA’s new Variation Fees Calculator are available.
To follow the blog click here.
The MHRA are also open to receiving feedback on the blog and will continue to develop the tool into a key source of information for users. If there is a topic that you think is worth covering, let the MHRA know!