RegDesk News/Info
The article outlines the key points associated with the classification rules for medical devices.
BfArM
The Federal Institute for Drugs and Medical Devices (BfArM), the German regulating authority in the sphere of healthcare products, has published a notice dedicated to notifications of interruptions or terminations of the supply of medical devices the parties responsible should submit in order to communicate the crucial information to all the stakeholders involved.
FDA
The article describes in detail the recent regulatory updates pertaining to medical device registration procedures in Taiwan.
Korea
The document provides an overview of the existing legal framework for innovative medical devices intended to be marketed and used in Korea.
DRAP
The article provides a general overview of the electronic reporting requirements in Pakistan.
