As part of FDA's mandate to protect the public health, CDRH provides information for regulated industry on determining how to comply with the federal laws and regulations governing medical devices. This information is provided in many forms including guidance documents on specific topics or devices, major web pages such as Device Advice, and online, interactive learning. CDRH is committed to educating industry on the relevant policies and regulations.
Industry Educational Resources
Overview of Medical Devices and Their Regulatory Pathways Guidance Documents (Medical Devices and Radiation-Emitting Products) CDRH Learn Device Advice: Comprehensive Regulatory Assistance Electronic Product Radiation Control Program CDRH Fiscal Year 2015 (FY 2015) Proposed Guidance Development and Focused Retrospective Review of Final Guidance[ARCHIVED] eSubmitter Tutorial Videos Acronyms and Abbreviations Search
- Medical Devices Advisory Committees
- Radiation-Emitting Products Advisory Committees