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HHS Publication FDA 818025 Reproduction/Document is OutofPrintConference of Radiation Control Program Directors, Inc. Guides for Naturally Occurring and AcceleratorProduced Radioactive Materials (ARM)Published
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The HHS publication FDA 81-8025 is a form used to report adverse events related to medical devices.
Manufacturers, importers, and device user facilities are required to file HHS publication FDA 81-8025.
HHS publication FDA 81-8025 can be filled out online on the FDA's website or submitted via mail.
The purpose of HHS publication FDA 81-8025 is to ensure that adverse events related to medical devices are reported and tracked for safety monitoring purposes.
Information such as the type of device, date of adverse event, details of the event, and patient information must be reported on HHS publication FDA 81-8025.
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