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CDRH Regulatory Educational Materials

The Division of Industry and Consumer Education (DICE) at the FDA’s Center for Devices and Radiological Health (CDRH) has developed the resources below to provide you with informative updates about medical devices and radiation-emitting electronic products.

Watch the CDRH Industry Basics Workshop: Understanding Risk with Medical Devices

If you missed the November 15, 2022, live broadcast of the CDRH Industry Basics Workshop on Understanding Risk with Medical Devices, view the recording.

Device Advice

Recently Posted Program Updates

• Standards and Conformity Assessment Program (11/15/2022)
• Total Product Life Cycle Advisory Program (TAP) (12/29/2022)
• ASCA-Accredited Testing Laboratories (01/04/2023)
• Voluntary eSTAR Program (01/11/2023)

CDRH Learn

CDRH recently posted the following educational modules:

Postmarket Activities section (under “Overview of the Quality System”)

• Risk Basics for Medical Devices
• Application of Risk Management Principles for Medical Devices

Contact DICE

Learn more about educational resources for you. If you have questions about DICE, please Contact Us – Division of Industry and Consumer Education (DICE).