SUBPART D—Responsibilities of Sponsors and Investigators (§312.50 to §312.70)
- 312.50—General responsibilities of sponsors.
- 312.52—Transfer of obligations to a contract research organization.
- 312.53—Selecting investigators and monitors.
- 312.54—Emergency research under § 50.24 of this chapter.
- 312.55—Informing investigators.
- 312.56—Review of ongoing investigations.
- 312.57—Recordkeeping and record retention.
- 312.58—Inspection of sponsor's records and reports.
- 312.59—Disposition of unused supply of investigational drug.
- 312.60—General responsibilities of investigators.
- 312.61—Control of the investigational drug.
- 312.62—Investigator recordkeeping and record retention.
- 312.64—Investigator reports.
- 312.66—Assurance of IRB review.
- 312.68—Inspection of investigator's records and reports.
- 312.69—Handling of controlled substances.
- 312.70—Disqualification of a clinical investigator.