The International Medical Device Regulators Forum (IMDRF) currently has four open consultations. These are opportunities for people to comment on work underway. The consultations are available at http://www.imdrf.org/consultations/consultations.asp
Each consultation includes documents, a comment sheet, and an e-mail address to send the comments.
The consultations are, with their closing dates:
Regulated product submission (RPS) Table of contents, June 21, 2013
Auditor competency and training requirements for organizations undertaking audits of medical device manufacturers, June 14, 2013
Recognition and monitoring of organizations undertaking audits of medical device manufacturers, June 14, 2013
UDI System for Medical Devices, July 31, 2013