The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has announced sweeping changes to regulations governing clinical trials, which it says are the largest in more than 20 years.

The International Recognition Procedure (IRP) – which went live on 1st January – means that the MHRA can take into account the expertise of trusted regulatory partners in other countries when ...

The table is limited by our hospital pharmacy's formulary; however, our purpose was to update the current literature. The table is intended for use as a guide when medications labeled for ...

In short, when discussing 'Clinical Trials' it's always best to check what definition others are using. Applications to the MHRA are generated via IRAS. For a CTIMP, selecting option 1 on filter ...

This tutorial is based upon the guidelines produced by the MHRA for their own publications, which have subsequently been adopted by an increasing number of other writers. These guidelines are set out ...