Criticality of Medical Device Risk Management for Patient and Product Safety 19 May 2021
Regulatory bodies have emphasised 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 organisation including post-market considerations will be discussed and outlined.
Presenter: Yervant Chijian, Brandwood CKC