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Any Location (virtual event)
1
Medical Device Single Audit Program — Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan
12 Mar 2025 • San Jose, Any Location (virtual event)
Organizer:
ComplianceOnline
Abstract:
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.
Contact:
Event Manager;     Phone: [+1-888-717-2436];     Email: sshastry@complianceonline.com
Topics:
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
Event listing ID:
1655039
Related subject(s):
Regulation in Medicine and Pharmacology
Event website:
https://www.complianceonline.com/medical-device-single-audit-program-mdsap-implementation-regulatory-processes-us-canada-brazil-australia-japan-seminar-training-80493SEM-prdsm?channel=conference-service


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Last updated: 12 February 2025