WEBINAR: CRITICALITY OF MEDICAL DEVICE RISK MANAGEMENT FOR PATIENT AND PRODUCT SAFETY

May 19, 2021
3:00 pm
Virtual

NOTE: This pre-recorded webinar is will be published on May 19, 3:00 PM MT.

Regulatory bodies have stressed 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, including best practices for implementing risk management activities and post-market considerations.

If you have questions on this topic, please submit them to help@brandwoodckc.com by May 13.

Please register to receive the recording directly to your inbox.

Register/Info