Understanding ISO 13485-FDA Requirements for Medical Devices 2015
18 Aug 2015
Webinar
Description
Topics
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?
Who should Attend
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
Past Events
Understanding ISO 13485-FDA Requirements for Medical Devices 2015 - 18 Aug 2015, Webinar (53463)
Important
Please, check "Understanding ISO 13485-FDA Requirements for Medical Devices" official website for possible changes, before making any traveling arrangements
