UK Supports End-To-End Management Of Trials Undergoing Combined Reviews

Ongoing efforts by the UK to deliver a single decision on the ethical and regulatory approval of new clinical trial applications have reached a major milestone ahead of the 2022 mandatory deadline. 

Clinical trials
The UK Is Looking to improve the speed and efficiency of clinical research approvals • Source: Shutterstock

IRAS, the UK portal for submitting clinical trial applications to the Medicines and Healthcare products Regulatory Agency (MHRA), has been updated to support the seamless lifecycle management of trials that are being voluntarily submitted by sponsors to undergo combined regulatory and ethics reviews.

The use of the combined review pathway is currently optional, although from January 2022 it will become mandatory for all...

Pink Sheet Podcast

Learn what's happening at the US FDA. On the go.

Derrick Gingery and the team bring you a weekly "Drug Fix".

More from United Kingdom

More from Europe