Subjgrp 72. General Requirements of This Subpart

• § 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?