Regulation of AI in Healthcare
Call for evidence outcome on the regulation of AI in healthcare. This represents the MHRA's position on regulating AI-enabled medical devices and healthcare innovations following public consultation.
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 Review the draft guidance or proposal at the official source, prepare comments identifying any practical impacts on your operations or products, and submit.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 ↗