How to Protect Your IP in Court: An Event Led by IPEC Judges Do you advise rights holders, support small businesses or creatives, or do you simply want to understand how the Small Claims Track works? Join the IP Crime Group for an online knowledge‑sharing session exploring the Small Claims Track of the Intellectual Property Enterprise Court (IPEC). IPEC specialises…
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February 20, 2026 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
How do you prove that your AI systems work as intended – not just say that they do?
As AI is more embedded in products, services, and decision-making, companies are under pressure to demonstrate responsible governance, transparency, and performance. Regulators, customers, and partners increasingly expect evidence to base their trust on. Our upcoming BSI webinar, ‘AI Governance and Assurance – Practical Steps to Prove Your AI Works as Intended’, explores how organizations can respond to this challenge in…
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February 19, 2026 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, UK Government Updates Regulatory Affairs Newsletter, UK Government Updates Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
Support your business by signing up for our IP workshop in Manchester
Join the Intellectual Property Office for a one day CPD accredited workshop that will help you understand how intellectual property (IP) can support your business. The workshop is led by our Business Outreach Team, who work with businesses across the UK to help them get to grips with IP in a clear and practical way. Event details Date: 25 February…
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February 19, 2026 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
Medical Device Regulations in Mexico 2026
Thursday, February 26, 2026 | 9:00 AM – 10:00 AM (CST) Mexico’s regulatory landscape for medical devices is shifting fast. With major updates to equivalency pathways, immediate approval modifications, GMP standards, and COFEPRIS leadership changes, global manufacturers need clarity now more than ever. Join us for an expert-led webinar featuring Pedro Sánchez Neri, Consulting Manager at Emergo by UL, who…
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February 6, 2026 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
Countdown to compliance: new UK clinical trial transparency requirements webinar
Countdown to compliance: new UK clinical trial transparency requirements webinar Our Head of Policy and Engagement, Clive Collett, is joining a panel of speakers at a webinar about upcoming changes to research transparency requirements as part of the amended clinical trials regulations. The webinar, organised by Citeline, takes place on Wednesday 25 February from 3pm to 4pm (UK time). Attendees…
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February 3, 2026 in Membership News, Membership News Archive, Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
NIHR: Introduction to the EU Diagnostic Medical Devices Regulation (EU) 2017/746 – Online interactive workshop
🕰️ Tuesday, 24 February 2026, 10am to 12pm Are you developing a in vitro diagnostic device for the health sector? Are you unsure if you need to adhere to the In Vitro Diagnostic Medical Device Regulations? Or what the risk classification of your device is according to the In Vitro Diagnostic Medical Device Regulations? Or which requirements your device need…
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January 23, 2026 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
QServe and TUV SUD – Navigate AI in MedTech: Live Regulatory Insights
We'd like to invite you to a live, practical webinar on Ensuring Quality in AI Driven Devices, hosted by Qserve experts and a guest speaker from Notified Body TÜV SÜD. We will unpack the regulatory expectations, explain what TÜV SÜD assesses during a submission review, and share examples from real-world cases, including those involving AI-supported clinical evaluation activities. Thursday, January 29,…
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January 23, 2026 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
Join Us: Shaping the Future of Clinical Trials in the Philippines – Exclusive Webinar
Dear Partners, We are delighted to invite you to our upcoming webinar, “Shaping the Future of Clinical Trials in the Philippines,” hosted by the IQVIA Philippines team. Date: Wednesday, February 4, 2026 Time: 9:30 pm – 10:30 pm SGT | 9:30 am – 10:30 am EST Join us for an insightful session featuring distinguished speakers from the Department of Health, Philippines FDA, and leading…
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January 15, 2026 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, UK Government Updates Regulatory Affairs Newsletter, UK Government Updates Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
Registration is now open for the Clinical Trials (CTs) with in vitro Diagnostic (IVD) devices webinar
Dear Colleagues, We are delighted to invite you to the Clinical Trials (CTs) with in vitro Diagnostic (IVD) devices webinar on Tuesday, 3 February 2026 from 14:00-15:00 (GMT). During this webinar the MHRA will present guidance and advice to sponsors who are submitting clinical trials with in vitro Diagnostic (IVD) devices. The webinar will be presented in sections including: Clinical Trials with IVDs The…
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December 22, 2025 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
WIPO webinar: Filing and managing PCT applications through ePCT
From 1st January 2026, ePCT will be the only way to digitally file PCT applications where Intellectual Property Office (IPO) UK is the receiving office. To help you prepare for this change, the World Intellectual Property Organization (WIPO) is hosting a 2-hour webinar on 18 December 2025. What you'll learn The webinars will show you how to: file international (PCT)…
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December 12, 2025 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, UK Government Updates Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter
Webinar on filing and managing PCT applications with WIPO and CIPA
Filing and managing PCT applications webinar with WIPO and CIPA From December 2025, ePCT will be the only way to file PCT applications where Intellectual Property Office (IPO) UK is the receiving office. The Chartered Institute of Patent Attorneys (CIPA) and the World Intellectual Property Organization (WIPO) are hosting two webinars to help you get familiar with the system. What…
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November 13, 2025 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
Improve your URRA with Expert Advice
Open Forum: Use-Related Risk Analysis Q&A Tuesday ,Nov, 18, 2025 | 9:00 AM - 10:00 AM CST Join our subject matter experts, Merrick Kossack, senior research director; Frauke Schuurkamp, managing human factors specialist; and Rachel Aronchick, managing human factors specialist, from Emergo by UL’s Human Factors Research & Design team on Nov. 18, 2025, from 9–10 a.m. CST for…
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October 22, 2025 in European Commission Updates Regulatory Affairs Newsletter, European Commission Updates Regulatory Affairs Newsletter Archive, Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
Eudamed Workshop – 3rd December 2025, Brussels
Introduction to the EUDAMED Workshop The European Commission is organising two free hybrid workshops to support the onboarding of all concerned actors to EUDAMED, in preparation for the mandatory use of Actors, UDI/Devices, Notified bodies and Certificates and Market surveillance modules. The workshop provides an overview of the obligations under the Medical Devices Regulations (Regulation (EU) 2017/745 — MDR, and Regulation (EU) 2017/746 — IVDR). These workshops are a…
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September 25, 2025 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
Premarket to Postmarket: Navigate Global Cybersecurity Expectations with Confidence
Strategic Cybersecurity for Regulatory Success—Are You Aligned? 12 and 14 November 2025 • 9:00 AM - 5:00 PM ET • 12.0 RAC Credits Health authorities spanning the US, European Union, Australia, Canada, and Japan have issued cybersecurity guidance that is essential for regulatory affairs professionals to understand. In addition to premarket concerns, some of the guidance also includes…
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September 25, 2025 in Industry Newsletters Regulatory Affairs Newsletter, Industry Newsletters Regulatory Affairs Newsletter Archive, Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
UK NEQAS Microbiology and Parasitology webinar on POCT
UK NEQAS is holding a six-part pan-disciplinary webinar series Quality Standards in Point of Care Testing. The second webinar will take place on 1 October 2025 and registration is now open at https://us06web.zoom.us/webinar/register/WN_a1-uMaqNThitDqJ0F-k1OA The webinar will include the following presentations – Professor Peter L. Chiodini Malaria Antigen Rapid Diagnostic Tests, what a dipstick! With apologies to "Only Fools and Horses”…
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September 12, 2025 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
Big Changes Coming: North American Packing Laws…
Thursday, September 18 10 AM ET / 7 AM PT / 4 PM CET Extended producer responsibility (EPR) laws are moving fast across the U.S. and Canada, and manufacturers are already on the hook for product end-of-life management. The cost of inaction? Fines, lawsuits, and potential loss of market access. Join our upcoming webinar to get clear on what these…
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