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The International Medical Device Regulators Forum (IMDRF) recognizes that a global approach to auditing and monitoring the manufacturing of medical devices could improve their safety and oversight on an international scale.
Why should you Attend:
Today with a single audit, it is possible for a medical device manufacturer to satisfy the quality management system requirements of Australia, Brazil, Canada, Japan and the USA! This is the benefit of the Medical Device Single Audit Program, or MDSAP. However, there are some vital considerations before embarking upon this approach to satisfying the regulators of five major markets.
Areas Covered in the Session:
Origin of MDSAP
Applicability of MDSAP
Advantages of MDSAP
Disadvantages of MDSAP
Who Will Benefit:
Corporate Management (Presidents, CEOs, COOs)
Quality Management (Vice Presidents, Directors, Managers)
Regulatory Management (Vice Presidents, Directors, Managers)
Sales & Marketing Management (Vice Presidents, Directors, Managers)
Event Fee: One Dial-in One Attendee Price: US$150.00
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