REGULATION
Investigational New Drug Application
ABSTRACT — EDITORS' SUMMARY
The IND regulation. Subpart D covers sponsor responsibilities including monitoring, recordkeeping, and adverse event reporting.
STATUTE · CANONICAL SOURCE
Read on canonical statute source www.ecfr.gov ↗ METADATA
SOURCE
LINK · CANONICAL LINK https://www.ecfr.gov/current/title-21/chapter-I/subchapter-D/part-312 ↗ RELATED · SAME AUTHORITY