Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices: 2-day In-person Seminar

This course includes:

- An easy to understand presentation of the auditing process as well as the requirements to audit under ISO 13485 and the FDA Quality System Regulation (cGMP).
- Discussions on auditing skills and hands-on auditing exercises.
- Review of the requirements for Quality Management Systems (QMS) for both the FDA (QSR/cGMP) and ISO 13485.
- Best practices for creating and managing a value-added auditing process that will meet both company business needs and regulatory r ...

Last Published: December 18, 2014 by Jim

Category: Healthcare and Medical