Submitting Reports and Requirements for Maintaining Records for Radiation

How to submit electronic product reports Reports of problems and hazards Required reports Variance applications

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Getting a Radiation Emitting Product to Market: Frequently Asked Questions

General Requirements Requirements for Records and Reporting Acknowledgement Letters and Accession Numbers Performance Standards and

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MQSA Insights

Welcome to MQSA Insights. These pages provide information pertaining to the Food and Drug Administration’s

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Search for a Certified Facility

This list of FDA Certified Mammography Facilities is updated weekly. If you click on Search for

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FDA Radiological Health Program

The mission of the FDA’s radiological health program is to protect the public from hazardous

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Resources for You (Radiation-Emitting Products)

This page provides links to information on radiation-emitting products for patients, consumers, health care professionals,

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News and Events (Radiation-Emitting Products)

News and Resources CDRHNew – News and Updates CDRH Events – This page provides information on webinars, meetings, workshops,

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Electronic Product Radiation Control Program

FDA is responsible for regulating radiation-emitting electronic products. The agency’s goal is to protect the

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Mammography Quality Standards Act (MQSA) and MQSA Program

UPDATES: On September 10, 2024, the FDA updated Important Information: Final Rule to Amend the Mammography

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Radiation Safety

FDA’s Center for Devices and Radiological Health (CDRH) radiation safety programs involve enforcement of mandatory

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