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]

Testimonials

Having just completed the very informative API and Clinical Trail course (thank you Shankar) I was reminded of the traps we can fall into whereby we try to keep ourselves in our little boxes. At the MHRA symposium, I have heard several times comments such as:- “no, I’m not doing the GMP day as it’s not relevant to me” or “GDP? Oh, that doesn’t apply to us as we are manufacturers”. I am sure these comments were made well out of the earshot of MHRA personnel and on the face of it see… Read more
API and Clinical Trails Training