The Future of Medical Device Regulation
The Future of Medical Device Regulation, on the 16th of September, the Medicines and Healthcare products Regulatory Agency (MHRA) launched a 10- week
Deadline Approaching – Medical Device Registration
Deadline approaching – Medical Device Registration for registering Class IIa and Class IIb (other than implants) products with the MHRA is the end of August 2021.
WDA(H) & Import – New Guidelines:
Following Brexit and GB leaving the EU the MHRA have advised that GB wholesale dealers now need to appoint an RPi
New Contract RP introduction
New Contract RP says hello! Please allow me to introduce myself as the newest member of PCL’s Contract RP Team.
Export & WDA(H) – Updated Guidelines:
As Great Britain (GB) are no longer part of the European Union (EU) since the 1st of January 2021 exit date. It is essential to ensure all the necessary changes have been made to remain MHRA compliant.
Keep up with changes in UK Medicines Laws and the requirements of Contract, Licence and Authorisation holders.
The Human Medicines Regulations is the main medicines law in the UK and they…