Essential Field Safety Notices: Key Updates from 2–6 June 2025
In early June 2025, a series of Field Safety Notices were issued highlighting updates and recalls for medical devices across […]
In early June 2025, a series of Field Safety Notices were issued highlighting updates and recalls for medical devices across […]
Meta description: A new white paper highlights essential observations from the 23rd IMDRF Session Joint Workshop on enhancing post-market activities
On October 2, 2025, Opella Healthcare UK LTD issued an urgent notification regarding a packaging error for the outer carton
Swissmedic has issued an urgent announcement concerning the recall of a specific batch of the veterinary medicine Revozyn RTU 400
Meta description: Maxearn Limited recalls Inhixa 12,000IU injection due to carton labeling error. Learn about the issue, impact, and actions
The International Medical Device Regulators Forum (IMDRF) has released a vital progress document detailing advancements under its 2021-2025 Strategic Plan.
On October 2, 2025, Swissmedic announced a key update to the Swissdamed UDI Devices module. The new discard functionality enables
The Medicines and Healthcare products Regulatory Agency (MHRA) has released its May 2025 Safety Roundup, providing updated safety guidelines and
The International Medical Device Regulators Forum (IMDRF) has introduced a convenient way for clinical, quality, and regulatory professionals to stay
Swissmedic has announced an important update for stakeholders involved in authorisation procedures for human medicinal products. Starting soon, a new