CMDCAS Certification and the Canadian MDR
This complimentary webinar provides insights about the Canadian Medical Devices Regulations (CMDR) and explains the process for CMDCAS Certification. Our presenters will identify each of the unique requirements that differentiate CMDCAS from standard ISO 13485 certification. In addition, they will provide practical advice on how to organize your technical documentation to simultaneously meet the requirements of Health Canada and the future European Medical Device Regulations.
Topics include:
● Organization of the CMDR
● Mandatory Problem Reporting
● Recalls
● Distribution Records
● Medical Device Licenses
● Establishment Licenses
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Presenters
Rob Packard Medical Device Academy, Inc.
Ron M. Mathis SGS
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