BSI’s Overview of CMDCAS provides information on the guidelines of the Canadian Medical Devices Conformity Assessment System (CMDCAS) and on how it will affect business in Canada. An experienced instructor will lead participants through exercises and discussion points, and participants are encouraged to ask specific questions during the webinar about the industry or the system as it applies to their organizations.
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
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.
System requirements
An internet connection with at least Microsoft Internet Explorer 5 or Netscape 5. Also, Corporate Firewalls may prevent the dowload of the MP3 Audio file which can cause the course to hang. Only your IT department can determine if MP3's are being blocked.
