Skip to main content
search
Category

Upcoming Events Regulatory Affairs Newsletter Archive

Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming Events Regulatory Affairs Newsletter Archive

TEAM-NB IVDR Technical Documentation training for Manufacturers

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/
admin
March 19, 2026
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming 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…
admin
March 19, 2026
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming 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…
admin
March 19, 2026
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming 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…
Ben Kemp
March 13, 2026
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming 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…
Ben Kemp
March 13, 2026
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming 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…
Ben Kemp
March 9, 2026
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming 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…
Ben Kemp
February 20, 2026
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming 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…
Ben Kemp
February 20, 2026
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUK Government Updates Regulatory Affairs NewsletterUK Government Updates Regulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming 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…
Ben Kemp
February 19, 2026
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming 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…
Ben Kemp
February 19, 2026
Close Menu