Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)? 2019 is a conference dedicated to medical Device Single Audit Program (MDSAP) requirements for the quality management system.
Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)? 2019 covers topics such as:
- Which Companies must have MDSAP?
- What is the Medical Device Single Audit Program (MDSAP)?
- Which Companies should postpone MDSAP?
- Which Companies should have MDSAP?
- How to implement MDSAP in a smart way into a quality management system according ISO 13485, 21 CFR 820 (QSR) or any other regulatory framework?
- What are the requirements of MDSAP?
- What is the difference between MDSAP and European Notified Body Audits?
- How the MDSAP-Audit is working?
Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)? 2019 brings together:
- Regulatory Affairs Managers
- CEO and top executives
- Quality Representatives
- Quality Managers
- Other managers, who need to deal with regulatory or quality guidelines