Report outlines UK strategy for regenerative medicines
This article was originally published in SRA
A new report has revealed how the UK government plans to ensure that the regulatory framework for regenerative medicines is "facilitating" and is supported by a strong intellectual property regime and appropriate standards"1,2.
You may also be interested in...
A draft EU guideline explains how disease registries can be used to supplement evidence in the pre-authorization phase and provide infrastructure for post-authorization evidence generation.
Companies are being encouraged to become “early adopters” of the EU Clinical Trials Information System when it goes live in December 2021.
Drug companies will be able to “play around” with the new EU Clinical Trials Information System in a secure testing environment before it goes live in approximately 15 months.