Top Management’s Responsibility for Risk Management in Medical Device Manufacturing (The Requirements of ISO 14971:2019)

This webinar is intended to be an overview, or an executive summary, of what Risk Management entails. It is written for Medical Device Manufacturing Top Management and explains what is expected of them throughout the Risk Management process. We will begin with a brief introduction to the concept of Risk Management and why it has become an expectation, integral with every aspect of the Medical device life cycle. We’ll then move on to each clause and take a bird’s eye view of what the expectation is for your company’s Top Management. We’ll also spend a few minutes on the Annex’s, and ISO 24971:2020 giving an overview of their value to Top Management’s development of risk management for medical device manufacturers.

Watch this webinar to know more about Top Management’s Responsibility for Risk Management in Medical Device Manufacturing