In my last post “Who’s watching your MedWatching”, I commented on some of the common issues manufacturers have with their MDR and complaint handling systems. It’s useful to know what people are doing wrong, but I think it is equally important to know how to solve those issues. So in this post, I’m going to point you to two very good resources that I found that give further insight into how to know if you have a problem, and how to fix your system.
[fa icon="clock-o"] 5/23/13 9:13 AM [fa icon="user"] Ryan Kasun [fa icon="folder-open'] Medical Device Report, Complaint Handling, MedWatch, Complaints, FDA, medical device, MDR, Adverse Event, Post Market Vigilance
Read More »Last year, FDA received almost one million adverse event reports from manufacturers1. Needless to say, the Office of Surveillance and Biometrics has been very busy, and so have manufacturers.
[fa icon="clock-o"] 5/3/13 7:11 AM [fa icon="user"] Ryan Kasun [fa icon="folder-open'] Medical Device Report, Complaint Handling, warning letter, MedWatch, Complaints, FDA, medical device, MDR, Adverse Event, Post Market Vigilance
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