Konferenzen  >  Medizin & Gesundheitswesen  >  Translationale Medizin, Klinische Studien  >  Virtuelle Veranstaltung

ComplianceOnline

This 3 hour webinar is focused on understanding the Medical Device Single Audit Program, the scope of the program, how to apply, the Authorized Organizations, the rating system developed and what you can expect when signing onto the program. The webinar will discuss how such audits are organized, what to expect during a MDSAP audit, how does this differ from a typical certified body audit, along with document movement and timeline expectations in receiving the facility’s certificate.

Event Manager;     Tel.: [+1-888-717-2436];     Email: sshastry@complianceonline.com

The Medical Device Single Audit Program (MDSAP), global medical device regulations seminar, medical device single audit program mdsap, GMP audit, mdsap audit, device classification, licensing pathways, medical device gmp, device labeling, medical device single audit program, medical device single audit program mdsap, fda medical device single audit program, medical device single audit program canada