The 23rd Management Committee Meeting of the International Medical Device Regulators Forum (IMDRF) took place in…
Category: Europe
europe updates on medical device regulation and quality.
Critical Updates: Field Safety Notices for Medical Devices Issued from 5 to 9 May 2025
Medical device users and healthcare teams should note the publication of new Field Safety Notices (FSNs)…
Key Learnings from the 23rd IMDRF Workshop: Enhancing Post-Market Surveillance in Medical Device Regulation
On September 30, 2025, the International Medical Device Regulators Forum (IMDRF), together with DITTA and GMTA,…
Important Regulatory Notification: Patient Safety Gaps Identified in Ipca Laboratories UK Ltd PILs
On September 30, 2025, Ipca Laboratories UK Ltd issued an urgent notification to the Medicines and…
IMDRF Releases Progress Update on Strategic Plan 2021-2025
The International Medical Device Regulators Forum (IMDRF) has provided a detailed progress report on its Strategic…
Critical Updates on Medical Device Field Safety Notices Issued from 18 to 22 August 2025
Between 18 and 22 August 2025, several Field Safety Notices (FSNs) were issued for medical devices,…
Stay Updated on IMDRF Developments: A New Way to Access Alerts
Attention clinical, quality, and regulatory professionals: the International Medical Device Regulators Forum (IMDRF) is making it…
Essential MHRA Updates: August 2025 Safety Guidance for Medicines and Medical Devices
The Medicines and Healthcare products Regulatory Agency (MHRA) has released its latest safety advice for August…
Review and Provide Feedback on IMDRF Regulatory Updates from the 24th Management Committee Session
The International Medical Device Regulators Forum (IMDRF) has announced updates from its Working Groups, which are…
Medical Device Field Safety Notices: Updates from August 25–29, 2025
Field Safety Notices issued between August 25 and 29, 2025, provide crucial updates for stakeholders involved…