Medical Device Consultancy
We are delighted to launch an updated Medical Device training and consultancy offering.
We are delighted to launch an updated Medical Device training and consultancy offering.
Let’s throw in some more cliches, there are still many plates spinning, balls in the air and how long is a piece of string?
Following the UK’s exit from the European Union (EU), the government identified a unique opportunity to improve how medical devices and in vitro diagnostic medical devices (IVDs) are regulated in the United Kingdom.
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?
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 for registering Class IIa and Class IIb (other than implants) products with the MHRA is the end of August 2021.