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Title 21

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eCFR Content

Editorial codification of the general and permanent rules published in the Federal Register.

Title 21 Food and Drugs Part / Section
Chapter I Food and Drug Administration, Department of Health and Human Services 1 – 1299
Subchapter D Drugs for Human Use 300 – 499
Part 312 Investigational New Drug Application 312.1 – 312.320
Subpart F Miscellaneous 312.110 – 312.145
§ 312.110 Import and export requirements.
§ 312.120 Foreign clinical studies not conducted under an IND.
§ 312.130 Availability for public disclosure of data and information in an IND.
§ 312.140 Address for correspondence.
§ 312.145 Guidance documents.