What is your Post-Market Surveillance Strategy

dr1vn

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#1
Was wondering what everyone uses as a Post-Market surveillance strategy.

Currently, I subscribe to the FDA warning letters. I was also thinking about setting up a google scholar alert to flag scientific literature that comes out that could involve my companies medical device.

Any other ways to "automate" the surveillance process?

What about other jurisdictions? Any suggestions on e-mail alerts that one could receive to conduct post-market surveillance in other countries?
 
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