14. BHTA, BIVDA, and PAGB updates on MHRA policy and UK medical device registration

Last Updated on 06/11/2025 by Sarah Sarsby

BHTA: See UK Medical Device Registration and CE/UKCA/NI Marking for an online version of this document and BHTA updates on the new UK regulatory regime as it unfolds; send regulatory queries to info@bhta.com.

BIVDA: BIVDA members can subscribe to the UKCA Sub-Group to receive email alerts relating to new information on the UK regulatory regime as it unfolds. Information is also communicated through the BIVDA Regulatory Newsletter. Regulatory queries can be sent to Regulatory@bivda.org.uk.

PAGB: PAGB members can access detailed regulatory intelligence on self-care medical devices from the PAGB website and subscribe to receive the regulatory intelligence newsletter. For more information on subscribing contact info@pagb.co.uk. Regulatory queries can be sent to regulatory@pagb.co.uk. PAGB also offers a regulatory consultancy service to companies seeking early advice; for example, on the viability of bringing a product to market, understanding requirements for medical device regulation or exploring claims. Contact us about our regulatory and advertising consultancy services. PAGB offers a wide range of training, including workshops, webinars, and eLearning courses such as the EU Medical Devices Regulation eLearning course. PAGB training can be found via the PAGB website.