Team NB are running a training course on EU IVDR Technical Documentation requirements for manufacturers. See below and attached IVDR Technical Documentation Training for Manufacturers On Thursday, 2026, July 2nd 9:00-17:00 CET (remotely) To register fill the form at the address: https://www.team-nb.org/manufacturertraining/ Link also available in NEWS: https://www.team-nb.org/new-session-ivdr-technical-documentation-training-for-manufacturers/
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March 19, 2026 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
US & EU Battery Compliance: What Manufacturers Need to Know [Webinar – March 25th, 2026]
Battery regulation is evolving rapidly across both the United States and the European Union. In the US, more states are introducing battery stewardship laws under EPR frameworks, creating an increasingly fragmented regulatory landscape. Meanwhile, the EU Battery Regulation (2023/1542) is introducing a single framework that expands compliance to cover the entire battery lifecycle. Join our upcoming webinar, 'Manufacturers’ Blueprint: Solving the…
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March 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 Brazil 2026
Brazil’s Medical Device Regulatory Landscape in 2026 Thursday, April 2, 2026 | 11:00 AM – 12:00 PM (Austin Texas, U.S.) This webinar will provide an essential update on Brazil’s evolving regulatory landscape, covering key changes taking effect in 2025 and what manufacturers should expect moving into 2026. Attendees will gain practical insights informed by Emergo by UL’s market entry and…
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March 13, 2026 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
The digital landscape in laboratory medicine
We would like to inform you of a new event proposed by LabMed members The digital landscape in laboratory medicine: Current systems, future possibilities, taking place on 30 April in Leeds. This one-day event will explore how laboratory IT systems work and how they can be utilised to support clinical decision-making, demand optimisation and safe, effective service delivery. The day will also…
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March 13, 2026 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
Town Hall – FDA’s Quality Management System Regulation (QMSR): Medical Device Risk-Based Inspections
Town Hall – FDA’s Quality Management System Regulation (QMSR): Medical Device Risk-Based Inspections The U.S. Food and Drug Administration (FDA) will host a town hall for industry and other interested parties to discuss the updated Inspection of Medical Device Manufacturers Compliance Program (CP) Manual (CP 7382.850), effective February 2, 2026. This CP includes the new inspection process, which aligns with…
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March 9, 2026 in Regulatory Affairs Newsletter, Regulatory Affairs Newsletter Archive, Upcoming Events Regulatory Affairs Newsletter, Upcoming Events Regulatory Affairs Newsletter Archive
Team PRRC EU AI Act Webinar
Team PRRC are running a webinar on the EU AI act and its impact on the MDR/IVDR framework: 🚨 New Webinar Alert – Organized by TEAM-PRRC 🚨 Navigating the EU AI Act: Practical Compliance Implications for PRRCs Artificial Intelligence is no longer a future topic for MedTech. It is now a regulated reality. With the entry into force of the EU AI…
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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
Do you want to understand how the Small Claims Track works?
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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