Medical Device Regulation Transition Timeline (MDR 2017/745)
Recording of the medical devices consultation webinar – Industry 5 October 2021
Medical device regulation and the MHRA devices registration system
What is the regulatory process for medical devices in the UK?
Ultimate guide to placing a medical device on the UK market
The truth about the UK vs EU situation
The new EU Medical Device Regulation EU MDR 2017/745 with Monir El Azzouzi
Changes to the Medical Devices Directives
Navigating the Red Tape - Discussing Regulatory updates for MedTech in the United Kingdom
What should you know on UKCA extension
Medical Device Regulations (MDR) Webinar | Recorded by BES Chairman Dirk ter Haar
How to Prioritize Documentation for MDR Transition Planning
Webinar // UKCA Requirements for Medical Device Manufacturers
Bristows reacts: the future regulation of medical devices in the UK
Tackling a Whirlwind of Uncertainties: UK Medical Devices Market Access
Attention! 1 year before UKCA is the law for Medical Devices in the UK
EU Exit and post-transition guidance, Regulation of Medical Devices Webinar - October 2020
Part 1: Medical Device Regulations
MedTech Intelligence: Now that the EU MDR deadline is passed, how do you sell your device abroad?
How to register Covid19 Medical Supplies? [Case Study UK MHRA]
