Medical Device: How To Identify, Address And Remove The Risks Of Labeling Product Recalls

Join medical device labeling and data experts from PRISYM ID and Reed Tech to find out the latest recalls trends from the industry, to hear about industry real-life scenarios and see how the right software platforms can help you deliver an effective strategy to minimize the risks of labeling recalls.

Every year, the FDA and MHRA recall medical devices due to labeling issues. To give you a better idea, labeling is no 5 in Top 10 Recall Root Causes in 2018.

Why is labeling such an important root cause in medical device recalls? It may be because many medical device manufacturers are still trying to resolve the issues in isolation, and not identifying the risks before product launches and not putting in place systems and procedures to avoid product recalls to happen.

Being pro-active proved beneficial for the organizations who looked at the cause and invested in market risk assessment platforms to identify and manage product risks or in validated labeling platforms which can offer complete label integrity to meet the strictest compliance requirements for FDA & EU regulations.

Key Learning Objectives:

• Develop an understanding of the common causes of labeling recalls and how they can be avoided
• Find out what are the medical device trends for product recalls
• Understand how manufacturers can meet the increasing compliance demands from both the FDA and European regulators
• Watch 15 min demo of practical examples of how Reed Tech’s Navigator™ for Medical Device Risk Assessment can help you
• Watch 15 min demo of practical examples of how PRISYM ID’s Label Management Software can help you