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Medical Device product approval, clearance, subsequent launch and continued market presence requires successful outcomes from regulatory inspections, notified body surveillance and certification audits.

With revisions in regulatory and standard requirements and the new age of virtual interfaces, an inspection readiness program is an essential tool in the Medical Device Quality System toolbox. This Webinar enables a perpetual state of readiness and delivers the level of confidence needed to confirm that your Quality System is in a state of control in the age of the New Normal.

Guest speaker, Augustine Smith, is a leader in Quality and Compliance with over 33 years of experience working with global regulations for compliance, quality systems and product quality for the Life Sciences. Joining her is our CSO, Nikki Willett. Together, they will share a five-phase approach to inspection readiness and why we need an innovative approach to quality and compliance today.

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