Federal (United States) · Regulations
Subpart D
12 sections
12 sections
- 21 C.F.R. § 312.50General responsibilities of sponsors.
- 21 C.F.R. § 312.52Transfer of obligations to a contract research organization.
- 21 C.F.R. § 312.53Selecting investigators and monitors.
- 21 C.F.R. § 312.54Emergency research under § 50.24 of this chapter.
- 21 C.F.R. § 312.60General responsibilities of investigators.
- 21 C.F.R. § 312.61Control of the investigational drug.
- 21 C.F.R. § 312.62Investigator recordkeeping and record retention.
- 21 C.F.R. § 312.64Investigator reports.
- 21 C.F.R. § 312.66Assurance of IRB review.
- 21 C.F.R. § 312.68Inspection of investigator's records and reports.
- 21 C.F.R. § 312.69Handling of controlled substances.
- 21 C.F.R. § 312.70Disqualification of a clinical investigator.