21 CFR Topic
General Requirements of This Subpart
June 25, 2020
§
1.690
How will FDA make information about recognized accreditation bodies and accredited third-party certification bodies available to the public?
§
1.691
How do I request reconsideration of a denial by FDA of an application or a waiver request?
§
1.692
How do I request internal agency review of a denial of an application or waiver request upon reconsideration?
§
1.693
How do I request a regulatory hearing on a revocation of recognition or withdrawal of accreditation?
§
1.694
Are electronic records created under this subpart subject to the electronic records requirements of part 11 of this chapter?
§
1.695
Are the records obtained by FDA under this subpart subject to public disclosure?
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