DICE Quarterly Newsletter - Vol. 2 Issue 1 -- Division of Industry and Consumer Education (DICE) | FDA

Contact Us -- Division of Industry and Consumer Education (DICE) | FDA

Get the Latest Regulatory Educational Materials from CDRH

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 the most current and accurate information about medical devices and radiation-emitting products. CDRH Learn CDRH recently released the following educational modules in CDRH Learn in these categories: How to Study and Market Your Device 513(g) Requests for Information (12/04/2019) Postmarket Activities Production and Process Controls, Part 2 (01/13/2020) Importing Medical Devices Into the United States (01/13/2020) Specialty Technical Topics Custom Device Exemption (11/27/2019) Radiation-Emitting Products Electronic Product Certification and Quality Testing Programs (01/13/2020) Would you like to see a new topic? Please give us your feedback! View CDRH Learn List of Modules Device Advice CDRH recently posted these pages in Device Advice: How to Study and Market Your Device (12/13/2019) How to Determine If Your Product is a Medical Device (12/16/2019) Importing and Exporting Medical Devices (12/31/2019) Exporting Medical Devices (12/31/2019) Types of Export Certificates (12/31/2019) How to Request Export Certificates or Permits and How To Submit Simple Notifications (12/31/2019) Exporting Medical Devices Frequently Asked Questions (FAQs) (12/31/2019) FDA Onsite Registration and Listing Verifications (12/31/2019) Other Export Documents (01/06/2020) Watch CDRH Industry Basics Program on 513(g) Requests and Custom Device Exemption

If you missed the live broadcast of the CDRH Industry Basics Program about 513(g) Requests for Information and Custom Device Exemption, view the recording. FDA Office of Regulatory Affairs presents “A Day in the Life”

In collaboration with DICE, FDA’s Office of Regulatory Affairs (ORA) has released a 5-module series introducing you to the ORA medical device program for inspections and related activities.  View modules. Medical Device Webinars, Stakeholder Calls, and More Educational Resources CDRH hosts regulatory webinars and stakeholder calls for the medical device industry. View past recordings and upcoming listings.  Learn more about educational resources for you.