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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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What is hhs publication fda 81-8025?
The HHS publication FDA 81-8025 is a form used to report adverse events related to medical devices.
Who is required to file hhs publication fda 81-8025?
Manufacturers, importers, and device user facilities are required to file HHS publication FDA 81-8025.
How to fill out hhs publication fda 81-8025?
HHS publication FDA 81-8025 can be filled out online on the FDA's website or submitted via mail.
What is the purpose of hhs publication fda 81-8025?
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.
What information must be reported on hhs publication fda 81-8025?
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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