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 ...

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 ...

We work closely with the Medicines and Healthcare products Regulatory Agency (MHRA) to make sure we can publish our guidance in a timely way. We aim to publish final guidance for all new technologies ...