Beginner (No knowledge at all of the topic).
Join our comprehensive course on Medical Device Single Audit Program (MDSAP) to gain a thorough understanding of the program’s fundamentals and prepare effectively for MDSAP audits. This course covers essential concepts, requirements, and audit preparation strategies to help you navigate the complexities of MDSAP successfully. Participants also gain insights into global medical device regulatory requirements.
Throughout the course, explore MDSAP’s history, terminology, and key players. Dive into MDSAP requirements, covering audit stages, non-conformity grading systems, escalation rules, and the certification cycle.
Discover the relationship between ISO 13485 and MDSAP, and explore country-specific QMS requirements for Brazil, the USA, Canada, Japan, and Australia. Navigate the MDSAP Audit Roadmap, exploring the seven process chapters in detail.
Receive practical guidance on audit planning and preparation, including strategies to streamline processes and documentation for seamless compliance with MDSAP requirements.
Join us and elevate your expertise in MDSAP compliance and audit readiness.
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