ISO 13485 Auditor Training PPT Presentation
Jul 22, 2022 04:49:46 AM
The requirements for the quality management system of organizations involved in one or more stages of the medical device life-cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities like technical support, etc.
For more information, you can visit here:
https://www.punyamacademy.com/