General Requirements of This Subpart | Midpage

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Code of Federal Regulations

ECFRab3e5ee91b62d40

General Requirements of This Subpart

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