MHRA Safety Features Team

by | Apr 3, 2017 | Blog, Falsified Medicines, MHRA, Regulation, WDA(H)

The Safety Features Team have set up a mail box for queries you might have regarding the new FMD requiring the registering of products onto the new EMVO portal:

[email protected]

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I attended one of the first virtual GDP Responsible Person Cogent “Gold Standard” training sessions due to the Covid-19 social distancing requirements. regardless of the circumstances the training was well organised and delivered to the required standard. This is why I recommended my associates to utilise PCL. Thank you Ryan, Sally, Adel and Jackie. Goncalo Sousa –  Quality Head UK at the Janssen Pharmaceutical Companies of Johnson & Johnson 05/05/2020
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