The first six EU reference laboratories for public health are now operational European Commission Updates Regulatory Affairs NewsletterEuropean Commission Updates Regulatory Affairs Newsletter ArchiveRegulatory Affairs NewsletterRegulatory Affairs Newsletter Archive

The first six EU reference laboratories for public health are now operational

The first six EU reference laboratories for public health are now operational Since 1 January 2025, the first six EU reference laboratories (EURLs) for public health have been operational and will now carry out activities for the next seven years. The EURLs, which bring together consortia of scientific expertise from across the EU, contribute to improving EU preparedness and ensuring…
Ben Kemp
January 9, 2025
Health Technology Assessment – Commission adopts rules for joint scientific consultations on medicinal products for human use European Commission Updates Regulatory Affairs NewsletterEuropean Commission Updates Regulatory Affairs Newsletter ArchiveRegulatory Affairs NewsletterRegulatory Affairs Newsletter Archive

Health Technology Assessment – Commission adopts rules for joint scientific consultations on medicinal products for human use

Health Technology Assessment - Commission adopts rules for joint scientific consultations on medicinal products for human use Recently, the European Commission adopted an implementing regulation setting out the rules for joint scientific consultations on medicinal products for human use at Union level, under the Health Technology Assessment (HTA) Regulation. The implementing act provides detailed procedural rules for the joint scientific…
Ben Kemp
January 9, 2025
Copyright and Artificial Intelligence Consultation Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUK Government Updates Regulatory Affairs NewsletterUK Government Updates Regulatory Affairs Newsletter Archive

Copyright and Artificial Intelligence Consultation

This consultation seeks views on how the government can ensure the UK’s legal framework for AI and copyright supports the UK creative industries and AI sector together. This consultation closes at 11:59pm on 25 February 2025 Access it here.
Ben Kemp
January 9, 2025
The Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024 Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUK Government Updates Regulatory Affairs NewsletterUK Government Updates Regulatory Affairs Newsletter Archive

The Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024

As promised by the MHRA, the Post Market Survailence Statutory Instrument 2024 No. 1368  modifying the UK MDR 2002 (as amended), has been published 16th December 2024, and there for applies for all IVD’s placed on the GB market from 16th June 2025. If you’ve not already started preparing your Quality Management systems for the update, now the time to…
Ben Kemp
January 8, 2025