About this document
Medical Device Supply Notification Rules by nonlastname is a document available to read on EtoBox.
Starting January 10, 2025, manufacturers must notify authorities of any interruptions or discontinuations of medical device supplies that could harm patients or public health, as mandated by EU regulations. Notifications should be sent to the relevant Member State authority and directly to economic operators and healthcare professionals. In Germany, notifications must be submitted electronically to the Federal Institute for Drugs and Medical Devices (BfArM) using a specific form provided by the European Com
- Author
- nonlastname
- Language
- EN