Common specification requirements for in vitro diagnostic devices
Information
Type
Closed consultation
Regulated products
IVDMD, Medical Devices
Topics
Health And Social Care
Published
May 21, 2024
Last updated
May 21, 2024
Description
MHRA seeks views on possible amendments to the Medical Devices Regulations 2002 to include common specification requirements for manufacturers of IVD devices.
Tags
Organization
Country / Region
United Kingdom
License
Open Government Licence 2.0 (United Kingdom)