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Crawler Documentation
Release the latest October 18, 2016Contents1Introduction32Installation53Tutorial
3.1 Quick start. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
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What is medcrawler documentation?
Medcrawler documentation is a reporting system for adverse events related to medical devices.
Who is required to file medcrawler documentation?
Manufacturers, importers, and device user facilities are required to file medcrawler documentation.
How to fill out medcrawler documentation?
Medcrawler documentation can be filled out online through the FDA's MedWatch portal.
What is the purpose of medcrawler documentation?
The purpose of medcrawler documentation is to track and analyze adverse events related to medical devices for public safety.
What information must be reported on medcrawler documentation?
Information such as the device model, patient harm, and event description must be reported on medcrawler documentation.
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