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WEBINAR: ISO13485: 2016 – An Overview of General and Product Realisation Requirements
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In 15 minutes, ascertain the major changes to the new ISO 13485:
- Impacts of the new revision
- New terminology
- General requirements
- Resource management
- Product realisation and design controls
- Q&A session
Led by Richard Young, trainer for MDTI's Managing the Transition to the new IVD Regulation and Practical Guidance for Medical Device Audits and Inspections courses.
- Impacts of the new revision
- New terminology
- General requirements
- Resource management
- Product realisation and design controls
- Q&A session
Led by Richard Young, trainer for MDTI's Managing the Transition to the new IVD Regulation and Practical Guidance for Medical Device Audits and Inspections courses.
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