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

Podden och tillhörande omslagsbild på den här sidan tillhör Brandwood CKC. Innehållet i podden är skapat av Brandwood CKC och inte av, eller tillsammans med, Poddtoppen.