General Requirements of This Subpart

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 M
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11. Subject Group General Requirements of This Subpart

Sections

• 1.690
  § 1.690 How will FDA make information about recognized accreditation bodies and accredited third-party certification bodies available to the public?
• 1.691
  § 1.691 How do I request reconsideration of a denial by FDA of an application or a waiver request?
• 1.692
  § 1.692 How do I request internal agency review of a denial of an application or waiver request upon reconsideration?
• 1.693
  § 1.693 How do I request a regulatory hearing on a revocation of recognition or withdrawal of accreditation?
• 1.694
  § 1.694 Are electronic records created under this subpart subject to the electronic records requirements of part 11 of this chapter?
• 1.695
  § 1.695 Are the records obtained by FDA under this subpart subject to public disclosure?