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.
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
Past Events
Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)? 2019 - 06 Mar 2019, Zurich, Switzerland (82303)
Important
Please, check "Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)?" official website for possible changes, before making any traveling arrangements
Event Categories
Business: Management, Quality assurance
Health & Medicine: Medical device, Medical laboratories, Medical technology
