Procedures for Modified Requirements and Exemptions

1. CFR
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3. Title 21
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5. Chapter I
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7. Part 1
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9. Subpart S
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11. Subject Group Procedures for Modified Requirements and Exemptions

Sections

Section numbering in the official eCFR can be non-consecutive. Omitted section numbers are not treated here as reserved unless the source explicitly labels them that way.

• 1.1360
  § 1.1360 Under what circumstances will FDA modify the requirements in this subpart that apply to a food or type of entity or exempt a food or type of entity from the requirements of this subpart?
• 1.1365
  § 1.1365 When will FDA consider whether to adopt modified requirements or grant an exemption from the requirements of this subpart?
• 1.1370
  § 1.1370 What must be included in a petition requesting modified requirements or an exemption from the requirements?
• 1.1375
  § 1.1375 What information submitted in a petition requesting modified requirements or an exemption, or information in comments on such a petition, is publicly available?
• 1.1380
  § 1.1380 What process applies to a petition requesting modified requirements or an exemption?
• 1.1385
  § 1.1385 What process will FDA follow when adopting modified requirements or granting an exemption on our own initiative?
• 1.1390
  § 1.1390 When will modified requirements that we adopt or an exemption that we grant become effective?
• 1.1395
  § 1.1395 Under what circumstances may FDA revise or revoke modified requirements or an exemption?
• 1.1400
  § 1.1400 What procedures apply if FDA tentatively determines that modified requirements or an exemption should be revised or revoked?