BSI’s Overview of CMDCAS provides information on the guidelines of the Canadian Medical Devices Conformity Assessment System (CMDCAS). An experienced instructor will lead participants through exercises and discussion points, and participants are encouraged to ask specific questions during the webinar.
Learning objectives
- Understand the origins of CMDR and CMDCAS, the market size, and the purpose of the scheme
- Learn about the process to achieve ISO 13485 registration
- Understand how management is expected to support this initiative
- Understand how to quantify the investment required for implementation
- Learn the prescribed timelines for implementation
- Learn how to keep informed of developments
Course materials
Students receive comprehensive course manuals with reference materials.
Who should attend
- Quality decision makers on management system strategy at medical device manufacturing firms
- Management team of medical device manufacturers
- Quality managers
- Auditors of medical device manufacturing firms (internal and external)
Prerequisite
General awareness of ISO 13485 and experience in a medical device manufacturing environment is recommended.
