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Ben Kemp

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8 May | UK Post Market Surveillance Regulations

Details: 🗓️ Date: 8 May 2025 ⏰ 4:00 - 5:00 PM CET | 3:00 - 4:00 PM GMT đź”— Register Now and Save Your Spot!   The latest UK Post-Market Surveillance Regulations will have significant implications for your business. Join our webinar to explore the purpose of the new regulations, the key changes, and the differences and impact on CE-marked…
Ben Kemp
April 23, 2025
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUK Government Updates Regulatory Affairs NewsletterUK Government Updates Regulatory Affairs Newsletter Archive

MedTech regulatory reform and the importance of partnerships

A new post, “MedTech regulatory reform and the importance of partnerships” has just been published on the MedRegs blog. Medical technologies will play a critical role in delivering the government’s 10 Year Health Plan and its three shifts: hospital to community; analogue to digital; and sickness to prevention. Risk-proportionate regulation, which ensures patient safety whilst supporting innovation and access. Read…
Ben Kemp
April 23, 2025
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUK Government Updates Regulatory Affairs NewsletterUK Government Updates Regulatory Affairs Newsletter Archive

Defra – Border Target Operating Model – getting it right at the border 10 04 25

Border Trade Newsletter – getting it right at the border  This newsletter from the Animal and Plant Health Agency (APHA) covers the latest operational updates on requirements and border controls for importing live animals, germinal products, products of animal origin and animal by-products into Great Britain. In this newsletter: FMD Austria update – Changes to fresh meat of ungulates listing…
Ben Kemp
April 23, 2025
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming Events Regulatory Affairs Newsletter Archive

Register now for Clinical Evaluation of Software as a Medical Device – 14 May 2025

Join us for our Clinical Evaluation for Software as a Medical Device webinar on 14 May 2025 This webinar will provide an overview of MDR requirements as applied to Software as a Medical device (SaMD). It will also aim to highlight common issues seen in the Clinical Evaluation of SaMDs. What will participants gain? Participants will gain an insight as…
Ben Kemp
April 23, 2025
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