Consultation on draft guidance for determining medical device application type
Public consultation on draft guidance to clarify how manufacturers determine the appropriate application type for medical device submissions. Aims to improve clarity in the application classification process.
Health canada 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 Review the draft guidance or proposal at the official source, prepare comments identifying any practical impacts on your operations or products, and submit.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 ↗