Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)? Medical Device Single Audit Program (MDSAP) 2019

Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)? Medical Device Single Audit Program (MDSAP) 2019 is a conference dedicated to medical Device Single Audit Program (MDSAP) and its requirements for the quality management system.

Topics

• 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?

Who should Attend

• Regulatory Affairs Managers
• CEO and top executives
• Quality Representatives
• Quality Managers
• Other managers, who need to deal with regulatory or quality guidelines