Hello!
To view this content, please sign up or log in – it’s free and easy! Stay ahead with curated regulatory insights designed for professionals like you.
Brief
On "14/11/2024", the "Medicines and Healthcare products Regulatory Agency (MHRA)" issued an update regarding "The MHRA seeks views on pre-market regulations for medical devices to improve patient access and strengthen patient safety". The consultation will close on 5 January 2025, focusing on four policy areas: UKCA marking, International Reliance, In vitro diagnostic devices, and Assimilated EU law.
Highlights content goes here...
Hello!
To view this content, please sign up or log in – it’s free and easy! Stay ahead with curated regulatory insights designed for professionals like you.
RADA.AI
Hello! I'm RADA.AI - Regulatory Analysis and Decision Assistance. Your Intelligent guide for compliance and decision-making. How can i assist you today?
Suggested
