Protecting the supply chain – New Supplier Qualification and the new MHRA GMDP database. Do you know that companies based in Great Britain no longer have their licenses and GMP/GDP certificates listed on the EUDRAGMDP database?
The Future of Medical Device Regulation in the UK- Do you know that the regulatory framework for the manufacture and supply of medical devices in the UK is changing?
API registration is an MHRA requirement if you manufacture, import or distribute active substances and you are based in the UK.
New Contract RP says hello! Please allow me to introduce myself as the newest member of PCL’s Contract RP Team.
