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Quality Systems Internal Audit for the Medical Device Industry
Discuss the Audit Life-Cycle and How to Enhance Current Processes
12-13 Jun 2018
Chicago, IL, United States of America
- Why You Should Attend
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Quality Systems Internal Audit for the Medical Device Industry
The internal audit function must continue to evolve as quality management systems advance and become more complex. Participants will discuss all elements of the auditing process, according to ISO 19011:2011, for use with ISO 13485:2016, to confirm that they are using the most efficient and effective tools and techniques. Achieving course objectives create additional value to any organization that needs to stay compliant and continue to be an industry leader.