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Code of Federal Regulations
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Title 21
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Chapter I — Food and Drug Administration, Department of Health and Human Services
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Subchapter D — Drugs for Human Use
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Part 314 — Applications for Fda Approval to Market a New Drug
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Subpart F — Subpart F [Reserved]
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Subpt. E
Hearing Procedures for New Drugs
Subpt. G
Miscellaneous Provisions
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Subpart F — Subpart F [Reserved]
Search Subpart F full text →
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Subpt. E
Hearing Procedures for New Drugs
Subpt. G
Miscellaneous Provisions
›
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