August 29 – 30, 2023
This two-day instructor-led course provides practical instruction for auditors and managers performing, facilitating, or managing internal and supplier audits against criteria contained within the European Union Medical Device Regulation (EU MDR). Learners will gain valuable knowledge on how to prepare for, plan, and conduct an internal or supplier audit based on the EU MDR. This course also focuses on ISO 13485:2016 relative to its correspondence with the EU MDR.
Who should attend:
This course is helpful for experienced internal auditors seeking to expand their auditing knowledge of the EU MDR, for managers of audit programs, and for anyone who will be the subject or participate in an EU MDR audit. Learners should have some internal audit experience and ideally have certified auditor/lead auditor qualifications in QMS audits.