Code of Federal Regulations (Last Updated: May 6, 2024) |
Title 21 - Food and Drugs |
Chapter I - Food and Drug Administration, Department of Health and Human Services |
SubChapter H - Medical Devices |
Part 812 - Investigational Device Exemptions |
Subpart C - Responsibilities of Sponsors |
§ 812.40 - General responsibilities of sponsors. |
§ 812.42 - FDA and IRB approval. |
§ 812.43 - Selecting investigators and monitors. |
§ 812.45 - Informing investigators. |
§ 812.46 - Monitoring investigations. |
§ 812.47 - Emergency research under § 50.24 of this chapter. |