European Union
The article provides a general overview of the UK regulatory framework for medical devices.
Medical Devices
Post-market surveillance (PMS) is a critical component of the European Union Medical Device Regulation (MDR).
RegDesk News/Info
The article outlines the key points associated with the classification rules for medical devices.
GMLP
The article describes in detail the regulatory requirements for certain innovative medical devices.
Medical Devices
Clinical evaluation is the cornerstone of the European Union Medical Device Regulation (MDR).
Medical Devices
The introduction of the European Union Medical Device Regulation (MDR) represents one of the most significant changes in the history of medical device regulation in Europe.
