Conference Description:

Attend this seminar to learn medical device quality management standard ISO 13485. It will cover the requirements for the quality management system, how a smart implementation of these requirements in the quality management system is possible and finally how the audit is working.
Learning Objectives:
What are the requirements of ISO 13485?
Which Companies must apply ISO 13485?
How to implement ISO 13485 in a smart way into a medical device quality management system?
How the ISO 13485-Audit is working?
Who will Benefit:
CEO’s
Regulatory Affairs
Quality Managers
Quality Assurance
Other managers, which need to deal with regulatory or quality guidelines