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Investigational New Drug Application (IND) | Midpage
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Code of Federal Regulations
Title 21
Chapter I
Subchapter D
Part 312
Subpart B
Investigational New Drug Application (IND)
312.20
Requirement for an IND.
312.21
Phases of an investigation.
312.22
General principles of the IND submission.
312.23
IND content and format.
312.30
Protocol amendments.
312.31
Information amendments.
312.32
IND safety reporting.
312.33
Annual reports.
312.38
Withdrawal of an IND.