Pre market medical devices regulation – stakeholder impact survey
MHRA is conducting a stakeholder impact survey regarding pre-market medical devices regulation. This is an open call for evidence from industry and other stakeholders on the impact of current regulatory requirements.
The mhra is inviting written submissions from manufacturers, sponsors, importers, and other industry stakeholders. Review the draft guidance or proposal at the official source, prepare comments identifying any practical impacts on your operations or products, and submit. Active participation helps ensure the final guidance reflects industry realities and gives your organisation early visibility of upcoming requirements.
View official source ↗