Overview:
The International Medical Device Regulators Forum (IMDRF) recognizes that a global approach to auditing and monitoring the manufacturing of medical devices could improve their safety and oversight on an international scale. At its inaugural meeting in Singapore in 2012, the IMDRF identified a work group to develop specific documents for advancing a Medical Device Single Audit Program (MDSAP).
The International Medical Device Regulators Forum (IMDRF) recognizes that a global approach to auditing and monitoring the manufacturing of medical devices could improve their safety and oversight on an international scale. At its inaugural meeting in Singapore in 2012, the IMDRF identified a work group to develop specific documents for advancing a Medical Device Single Audit Program (MDSAP).
Speakers
Shep Bentley,
Who Should Attend
- Corporate Management (Presidents, CEOs, COOs)
- Quality Management (Vice Presidents, Directors, Managers)
- Regulatory Management (Vice Presidents, Directors, Managers)
- Sales & Marketing Management (Vice Presidents, Directors, Managers)
