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Regulatory Affairs Newsletter

UK Government Updates Regulatory Affairs NewsletterUK Government Updates Regulatory Affairs Newsletter Archive

DSIT weekly update (WC 11 Dec)

Please note this is an extract of the original bulletin. Advai: Regulatory Aligned AI Deployment Framework  Page summary: Case study from Advai. Change made: First published. Advai: Implementing a Risk-Driven AI Regulatory Compliance Framework Page summary: Case study from Advai. Change made: First published. Advai: Assurance of Computer Vision AI in the Security Industry Page summary: Case study from Advai.…
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December 20, 2023
UK Government Updates Regulatory Affairs NewsletterUK Government Updates Regulatory Affairs Newsletter Archive

DBT weekly update (WC 11 Dec)

Please note this is an extract of the original bulletin. New unit to crack down on firms dodging Russian sanctions Page summary: Government announces new unit to clamp down on companies evading sanctions Change made: First published. Reference Documents for The Customs Tariff (Preferential Trade Arrangements) (EU Exit) Regulations 2020 Page summary: Find the UK’s preferential tariffs and Rules of…
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December 20, 2023
Industry Newsletters Regulatory Affairs NewsletterIndustry Newsletters Regulatory Affairs Newsletter Archive

UL Standards update (WC 30 Nov)

UL have published the following documents between 30 November and 15 December: Standard UL 2900-1 Ed. 2 Software Cybersecurity for Network-Connectable Products, Part 1: General Requirements CSDS Proposal UL 62133-2 Ed. 1 Secondary Cells and Batteries Containing Alkaline or Other Non-Acid Electrolytes - Safety Requirements for Portable Sealed Secondary Cells, and for Batteries Made from Them, for Use in Portable…
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December 20, 2023
FDA updates Regulatory Affairs NewsletterFDA Updates Regulatory Affairs Newsletter Archive

U.S. FDA weekly update (WC 18 Dec)

FDA publishes a draft guidance on Real World evidence FDA is issuing this draft guidance to clarify how FDA evaluates real-world data (RWD) to determine whether they are of sufficient quality for generating real-world evidence (RWE) that can be used in FDA regulatory decision-making for medical devices. This draft guidance also proposes expanded recommendations to the 2017 guidance, Use of Real-World…
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December 20, 2023
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ISO 13485 Stakeholder Feedback Survey

In follow up to the plenary discussions in December 2022, ISO/TC 210 (AAMI QM, Quality management and corresponding general aspects for products with a health purpose including medical devices) Working Group has begun preparatory work on items for future revision of ISO 13485:2016. The technical committee have launched a survey seeking feedback on the use of the standard for regulatory…
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December 20, 2023
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