Understanding ISO 13485-FDA Requirements for Medical Devices 2015 is a webinar that covers topics such as:
- Which areas are being revamped under ISO 13485: 2015?
- What is in store for currently marketed medical devices when ISO 13485: 2015 gets launched?
- What sort of gap analysis is a must?
- Where does one begin?
- When is your quality system expected to be completely switched over to cater to the changes being introduced?
Understanding ISO 13485-FDA Requirements for Medical Devices 2015 is intended for:
- Quality Assurance
- Quality and Regulatory Managers
- ISO 13485: 2015, Medical device regulations, Quality system for medical devices
- Supplier Management and auditing professionals in the medical device or medical device-pharmaceutical industry quality professionals all across the world