Register of Medical Devices – Through 2021, as part of the Brexit changes, medical device manufacturers and/or their UK agents have had to register all classes of devices with the MHRA.
We still have spaces available on our RPi course running on the 23rd of September starting at 10 am until 12:30 pm.
With the ever-changing climate around us, there is a lot of information to take in.
Shankar Seetharaman is a Qualified Person with many years of experience in API auditing and clinical trials supply. He currently is the Managing Director of Pharmanswers Ltd which is a consultancy with a proven track record of providing quality and regulatory support for the pharmaceutical industry…
Manufacturers, Wholesalers, Responsible Persons and Healthcare Professionals must consider how they communicate and what are the effective channels of communication they should consider to effectively get their message across.
The way the public is influenced is aided by technologies which facilitate messages to be spread at speed, and people trust the medias and or people who deliver the message often without question. They often sign up to follow their newfound friend who is now their trusted expert. People join groups and sign up to blogs and alerts and rarely question the bona fides.