IMDRF welcomes input and participation by medical device sector stakeholders. Participation takes places via a number of channels including:
- Participation in open member working groups
- Attendance and participation in the regular IMDRF open stakeholder forums
- Attendance as invited participants at IMDRF Management Committee meetings
The aim of IMDRF is to accelerate international medical device regulatory harmonization and convergence. For this to be achieved, close collaboration between regulators and stakeholders is essential, and in particular between regulators and the regulated industry.
Interested parties can signal their preliminary interest in attending the next open session in 2014 by contacting the IMDRF Secretariat at USA-IMDRF-SECRETARIAT@fda.hhs.gov.