Responsibilities of Sponsors

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. Medical Devices
  6. Investigational Device Exemptions
  7. Responsibilities of Sponsors

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Section
812.40

General responsibilities of sponsors.

Section
812.42

FDA and IRB approval.

Section
812.43

Selecting investigators and monitors.

Section
812.45

Informing investigators.

Section
812.46

Monitoring investigations.

Section
812.47

Emergency research under § 50.24 of this chapter.