The training program will provide insight into complying with the key QMS requirements for organizations selling medical devices in Canada.
Why Should You Attend:
This webinar will examine the relationship between the Canadian quality management system (QMS) regulations and the requirements contained in ISO 13485:2003. It will also offer insight into handling the most common quality QMS problem areas and discuss the revisions contained in the 2016 version of the standard.Areas Covered in the Webinar:
- Relationship between the Canadian quality management system (QMS) regulations and the requirements contained in ISO 13485:2003.
- Canadian QMS requirements in addition to the requirements contained in the standard (Refer: GD210: ISO 13485:2003 QMS Audits Performed by Health Canada Recognized Registrars).
- Insight into handling the most common quality QMS problem areas.
- A discussion of the revisions contained in the 2016 version of the standard.
- The Canadian medical device quality management system regulatory requirements
Who Will Benefit:
- Quality Professionals
- Quality Audit Managers
- Regulatory Professionals
- Production Managers
- Process Owners
- Project Managers
Course Provider
Edward Kimmelman,
