Webinar: Criticality of Medical Device Risk Management for Patient and Product Safety

Description

Regulatory bodies have emphasized the importance of Risk Management under ISO 14971 in the development of medical devices and in-vitro diagnostics. In this webinar, led by Senior Consultant, Yervant Chijian we explore how Risk Management is critical to regulatory frameworks and provide an overview of the fundamental principles and key standards. In addition, best practices for implementing risk management activities within your organization including post-market considerations will be discussed and outlined.

Presenter: Yervant Chijian, Brandwood CKC

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Wednesday 19 May
2pm USA Pacific / 5pm USA EDT

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