Medical Device 2020 - Upgrade Your Medical Device Recall Strategy

Recall situations are diverse and can be complex, often negatively impacting the larger business in many ways.
This despite regulatory, quality and service personnel executing the recalls according to their understanding of the regulations and your company’s internal processes.
An overview of FDA requirements for recalls of medical devices, analysis of guidelines and development of a recall strategy
Definitions of corrections vs. removals
A discussion of potential impacts of recalls or corrective actions in one or more geographical areas as part of a global business
Speaker:
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations.