It’s easy to see why any medical device company should be conducting regular risk assessments for its products. A thorough analysis of safety and quality data should influence the decisions made for multiple business initiatives, including risk management, post-market surveillance, and competitive intelligence.

There are many data sources containing device safety and quality information, but there are obstacles to effectively utilizing them. Because data is not normalized or standardized, it can be difficult to search and retrieve comprehensive results; establishing benchmarks and conducting comparisons across products – especially those of your competitors – sometimes feels impossible.

In this webinar, we’ll examine why regular risk analysis is so important, the data sources available, what the data can tell us, and how to leverage big data to deliver actionable insights.

Featured Speakers:

Nicolas Tasse-Guillen

Senior Product Manager
Reed Tech

Rachel Benway

Associate Product Manager
Reed Tech
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