Get the free www.accessdata.fda.gov scripts cdrhMAUDE - Manufacturer and User Facility Device Exp...
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Annual General meeting 2020 30th September 1:15 pm Via Zoom Minutes ANNUAL GENERAL MEETING 2020 1. To receive apologies for absence Present Glynis Wright (GW) Christ Hughes (CH) Mahmoud Duke (MD)
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This refers to the Center for Devices and Radiological Health (CDRH) Medical Device Adverse Event Reporting Program (MDR) database.
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The purpose of wwwaccessdatafdagov scripts cdrhmaude is to collect and store adverse event reports related to medical devices.
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Information such as device details, adverse event description, patient information, and reporter details must be reported on wwwaccessdatafdagov scripts cdrhmaude.
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