Background
Following the 2021 government consultation on changes to the Medical Devices Regulations 2002 (MDR 2002), and now armed with even more information and experience, on Nov. 14, the U.K. medical device regulator, the Medicines and Healthcare products Regulatory Agency (MHRA) announced the launch of a public consultation. The MHRA solicited members of the public, including patients, medical device researchers, developers, manufacturers and suppliers, clinicians and other healthcare professionals, to provide their views on proposals to update the following four areas for the future regulatory framework for medical devices.
MHRA Opens Public Consultation on Proposed Changes to Medical Device Regulatory Framework
MHRA Opens Public Consultation on Proposed Changes to Medical Device Regulatory Framework
U.K. MHRA invites members of the public to provide their views on proposals to update four areas of the legislation for medical devices in Great Britain.
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