Ben Kemp – Page 168 – BIVDA Newsletter

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

Brexit Update (WC 19 Jan)

Regulating medical devices in the UK Page summary: What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets. Change made: Updated to reflect the laying of The Medical Devices (Post-market Surveillance requirements) (Amendment) Regulations 2024. Time updated: 10:00am, 15 January 2025 Implementation of medical devices future regime Page summary:…

Ben KempJanuary 27, 2025

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

Department for Science, Innovation and Technology Update (WC 19 Jan)

AI Opportunities Action Plan Page summary: Recommendations for the government to capture the opportunities of AI to enhance growth and productivity and create tangible benefits for UK citizens. Change made: First published. Time updated: 10:21am, 13 January 2025 AI Opportunities Action Plan: government response Page summary: Government response to recommendations set out in the AI Opportunities Action Plan and the…

Ben KempJanuary 27, 2025

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

DBT Updates (WC 19 Jan)

Overseas business risk for Taiwan Page summary: Information on key security and political risks which UK businesses may face when operating in Taiwan. Change made: Guide updated overall. Time updated: 6:27am, 14 January 2025 Overseas business risk for Guinea Page summary: Information on key security and political risks which UK businesses may face when operating in Guinea. Change made: This…

Ben KempJanuary 24, 2025

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

DHSC Updates (WC 19 Jan)

Health and Social Care Secretary's statement: winter 2025 Page summary: The Health and Social Care Secretary made a statement to the House of Commons on winter pressures. Change made: First published. Time updated: 5:17pm, 15 January 2025 UK invests £5.5 million to tackle mpox in sub-Saharan Africa Page summary: £5.5 million to go towards vital research projects to tackle ongoing…

Ben KempJanuary 24, 2025

Environmental Newsletter Environmental Newsletter Archive UK Government Updates Environmental Newsletter UK Government Updates Environmental Newsletter Archive

DEFRA Updates (WC 19 Jan)

Foot and mouth disease in water buffalo in Germany Page summary: Preliminary outbreak assessment and updated situation assessments for foot and mouth disease (FMD) in water buffalo in Germany. Change made: First published. Time updated: 4:12pm, 14 January 2025 Animal diseases: international and UK monitoring Page summary: Monitoring for major, notifiable or new and emerging animal disease outbreaks internationally and…

Ben KempJanuary 24, 2025

Environmental Newsletter Environmental Newsletter Archive Upcoming Events Environmental Newsletter Upcoming Events Environmental Newsletter Archive

Unlock the Future of Product Circularity – Upcoming Requirements & Standards [Webinar – January 29th, 2025]

Emerging Circular Economy (CE) requirements are pushing manufacturers and their networks to measure and share product circularity information, which poses a key question: how exactly are you measuring and assessing your products' circularity and acquiring the necessary data? Join our expert webinar, Emerging Requirements & Standards for Measuring Product Circularity and Supply Chain Data Collection, where Walter Jager from ECD…

Ben KempJanuary 24, 2025

Environmental Newsletter Environmental Newsletter Archive MedTech Europe Updates Environmental Newsletter MedTech Europe Updates Environmental Newsletter Archive

For information: Consultation submissions: Microplastics & Non-Animal Testing

MedTech Europe has published two position papers. One of the reporting requirements for microplastics (approx. less than 5mm, although there is also a spec for filaments) reporting requirements and the other on the phase out of animal testing. Microplastics Reporting Requirements - link Non-Animal Testing - link

Ben KempJanuary 24, 2025

Environmental Newsletter Environmental Newsletter Archive European Chemicals Agency Updates Environmental Newsletter European Chemicals Agency Updates Environmental Newsletter Archive

CLP: ECHA public consultations

ECHA public consultations: call for comments ECHA has announced public consultations on the following proposals for harmonised classification and labelling (CLH) The Great Britain mandatory classification and labelling (GB MCL) process includes the consideration of information gathered from public consultations, conducted by HSE or international bodies such as the European Chemicals Agency (ECHA). Deadline: 7 February 2025 cyclohexa-2,5-dien-1-ylidene]dimethylammonium m-azo]benzenesulphonate (EC:…

Ben KempJanuary 24, 2025

Environmental Newsletter Environmental Newsletter Archive MedTech Europe Updates Environmental Newsletter MedTech Europe Updates Environmental Newsletter Archive

MedTech Europe Sustainable Corporate Governance Working Group – OECD (BIAC) Sustainability Reporting Survey

Please see below an email from the OECD (BIAC) Secretariat. They are asking for feedback to their ongoing survey on Sustainability Reporting experiences and challenges, you can find more information below in case you would like to participate. The deadline is the 30th January. In support of Business at OECD (BIAC)’s ongoing special project on “The Risks of Divergence between…

Ben KempJanuary 24, 2025

MedTech Europe Updates Regulatory Affairs Newsletter MedTech Europe Updates Regulatory Affairs Newsletter Archive Regulatory Affairs Newsletter Regulatory Affairs Newsletter Archive

Publication of the MedTech Europe 2024 Regulatory Survey Report

MTE are pleased to announce the publication of the MedTech Europe 2024 Regulatory Survey Report and Executive Summary. This comprehensive report provides valuable insights into the current regulatory challenges faced by manufacturers under the In Vitro Diagnostic Regulation (IVDR) and Medical Device Regulation (MDR). The findings highlight key concerns such as increased costs, regulatory unpredictability, and delays in conformity assessments,…

Ben KempJanuary 24, 2025