Did you know there were more than 2.5 million medical device adverse events reported in the last three years alone?

There’s a daunting amount of data out there about medical device quality and safety and my friends at Reed Tech will help you find and synthesize it at http://medgroup.biz/bigdata webinar on August 8.

Public sources such as FDA and private databases house valuable information about adverse events, recalls, inspection findings and warning letters. But this data can be difficult and time consuming to locate, standardize and compare.

We’ll examine the available safety and quality data sources, what they can tell us, challenges with analyzing the data, and what you can do to overcome these challenges and help you in your role.

This will also help you determine how you stack up against competitor products. In sum, it’s worthwhile to extract meaningful insights and monitor internal changes and market developments – and we’ll teach you on this webinar how to do it more effectively and where to begin.

Join us to learn about:
• Available safety and quality data sources
• What the data can tell us about a device or product portfolio
• Challenges with analyzing the data and how to overcome them
• How data analytics can help with Post-market Surveillance, Failure Mode Analysis, and Risk Analysis

Who should attend?
Leaders and Team Members from:
• Quality Assurance, Post-market Surveillance & Safety
• Research & Development, Engineering
• Business Development, Sales & Marketing
• Regulatory Affairs & Compliance

That link again, http://medgroup.biz/bigdata to learn how to find and process big data to keep your company growing.

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Next week’s webinar about Improving the Value of Your MedDev Company at http://medgroup.biz/value will discuss an algorithm to assess enterprise value and, based on your outcome, can tell you which management decisions will add the most incremental value.

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Make it a great week.

Joe Hage
Medical Devices Group Leader