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The Customs (Tariff and Miscellaneous Amendments) (No. 2) Regulations 2025

Not clear exactly how this impacts, as it references updated lists not in the notice, so difficult to see exactly which tariff codes etc. have been amended, but could impact import charges for raw materials. This is part of the regular updates of customs charges. The Customs (Tariff and Miscellaneous Amendments) (No. 2) Regulations 2025 These Regulations are made under…
Ben Kemp
July 4, 2025
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUK Government Updates Regulatory Affairs NewsletterUK Government Updates Regulatory Affairs Newsletter Archive

The Customs (Miscellaneous Amendments) Regulations 2025

Please not the changes being made to UK customs regulations, include postal packet and universal package services, including for items declared as temporarily being in the UK. The Customs (Miscellaneous Amendments) Regulations 2025 This instrument contains various amendments to Customs secondary legislation made under the Taxation (Cross-border Trade) Act 2018 (c. 22) (“TCTA”), and amendments to the Postal Packets (Revenue…
Ben Kemp
July 4, 2025
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUK Government Updates Regulatory Affairs NewsletterUK Government Updates Regulatory Affairs Newsletter Archive

Biocides: GB active substance renewal submission deadlines

Apply for active substance renewal by the deadlines to keep products on the GB market. Under the GB Biocidal Products Regulation (GB BPR), active substance approvals will expire unless a renewal application is submitted at least 550 days before their expiry date. The 550-day deadlines are coming up for the following active substance/product type combinations under GB BPR: 27 December…
Ben Kemp
July 4, 2025
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Clinical Trials update – June 2025

UK Health Research Authority are requesting feedback by 10th September on guidance to the new Clinical Trials Regulation. Note that the new regulation applies to medicinal products, however clinical trials involving combination products, or using IVDs are in scope, although you have to hunt through the Guidance and find the reference to: Combined trials of an investigational medicinal product and…
Ben Kemp
July 4, 2025
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MHRA publishes 2025 Business Plan

The Medicines and Healthcare products Regulatory Agency (MHRA) has published its Business Plan for 2025/26, reaffirming its commitment to keeping patients safe and enabling access to high quality and effective medical products through innovation across the UK. The plan appears forward-looking, acknowledging their purpose as an engine of economic growth and the need to be bold and ambitious in the…
Ben Kemp
July 1, 2025
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUK Government Updates Regulatory Affairs NewsletterUK Government Updates Regulatory Affairs Newsletter Archive

UK MHRA leads safe use of AI in healthcare as first country in new global network

UK MHRA leads safe use of AI in healthcare as first country in new global network Page summary: The MHRA will help shape international rules for AI in healthcare – speeding up access to safe, effective technologies into the NHS and worldwide. Change made: First published. Time updated: 2:20pm, 24 June 2025
Ben Kemp
June 26, 2025
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUK Government Updates Regulatory Affairs NewsletterUK Government Updates Regulatory Affairs Newsletter Archive

Update from GOV.UK for: UKHSA Presents

UKHSA Presents Page summary: UKHSA Presents is a new webinar series profiling the science behind how we prevent, prepare for and respond to infectious diseases and environmental hazards to keep all our communities safe. Change made: Updated next event details and added sign-up link. Time updated: 9:30am, 24 June 2025
Ben Kemp
June 26, 2025
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUK Government Updates Regulatory Affairs NewsletterUK Government Updates Regulatory Affairs Newsletter Archive

HRA Now – updated model Commercial Chief Investigator Agreement and CRO version published

What: the model Commercial Chief Investigator Agreement (mCCIA) has been updated based on feedback, a contract research organisation (CRO) version has been published  Who: Commercial sponsors, contract research organisations (CROs), NHS and HSC organisations employing Chief Investigators  Where: UK wide (England, Northern Ireland, Scotland and Wales)  When: Friday 20 June 2025  An updated version of the model Commercial Chief Investigator Agreement (mCCIA) has been published for…
Ben Kemp
June 26, 2025