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Ben Kemp

European Commission Updates Regulatory Affairs NewsletterEuropean Commission Updates Regulatory Affairs Newsletter ArchiveRegulatory Affairs NewsletterRegulatory Affairs Newsletter Archive

CELEX:32024L2749R(02): Corrigendum to Directive (EU) 2024/2749 of the European Parliament and of the Council of 9 October 2024 amending Directives 2000/14/EC, 2006/42/EC, 2010/35/EU, 2014/29/EU, 2014/30/EU, 2014/33/EU, 2014/34/EU, 2014/35/EU, 2014/53/

I’ve highlighted items below that may impact IVDs (and Vet and RuO products) (Bold) or those impacting Vet use and RuO products but not IVDs (Italics). Corrigendum to Directive (EU) 2024/2749 of the European Parliament and of the Council of 9 October 2024 amending Directives 2000/14/EC, 2006/42/EC, 2010/35/EU, 2014/29/EU, 2014/30/EU, 2014/33/EU, 2014/34/EU, 2014/35/EU, 2014/53/EU a View article... This relates to…
Ben Kemp
September 22, 2025
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUK Government Updates Regulatory Affairs NewsletterUK Government Updates Regulatory Affairs Newsletter Archive

Get ready for the biggest change to UK patent services

Get ready for the biggest change to UK patent services Big changes are coming to UK patent services, and we want to make sure you're fully prepared. Our new ‘One IPO Patent Service’ is launching in early 2026 transforming how you apply for and manage all your UK patents. To help you prepare for this major transition, we're publishing a…
Ben Kemp
September 22, 2025
MedTech Europe Updates Regulatory Affairs NewsletterMedTech Europe Updates Regulatory Affairs Newsletter ArchiveRegulatory Affairs NewsletterRegulatory Affairs Newsletter Archive

EUDAMED onboarding – Commission’s EUDAMED Workshops: 8 Oct, Rome, Italy; 3 Dec, Brussels, Belgium

Registration is open for the new workshops on EUDAMED, organised by DG SANTE, European Commission: 8 October 2025, Rome, Italy 🇮🇹 3 December 2025, Brussels, Belgium 🇧🇪 For in person or online participation, you can register here. The workshop programme and venues are displayed at the workshops page : Audience: economic operators, notified bodies, national authorities, and other stakeholders Content:…
Ben Kemp
September 22, 2025
Industry Newsletters Regulatory Affairs NewsletterIndustry Newsletters Regulatory Affairs Newsletter ArchiveRegulatory Affairs NewsletterRegulatory Affairs Newsletter Archive

The Customs (Tariff and Miscellaneous Amendments) (No. 3) Regulations 2025

The Customs (Tariff and Miscellaneous Amendments) (No. 3) Regulations 2024 Regulation 2 amends the definition of “the authorised use document” in regulation 32(2) of the Customs (Special Procedures and Outward Processing) (EU Exit) Regulations 2018 (S.I. 2018/1249) to refer to a new version of that document. The new version of this document removes one commodity code to align with changes…
Ben Kemp
September 22, 2025
European Commission Updates Regulatory Affairs NewsletterEuropean Commission Updates Regulatory Affairs Newsletter ArchiveRegulatory Affairs NewsletterRegulatory Affairs Newsletter Archive

European Commission launches consultation to streamline MedTech regulation

Please note that the EU has launched a follow up focused consultation on the streamlining of the EU MDR and IVDR. This is a more focused consultation following on from the previous consultation, and the EC are not intending to conduct a full review of the implementation of the MDR and IVDR. MedTech Europe are very focused on these consultations,…
Ben Kemp
September 22, 2025
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