Code of Federal Regulations · Section

§ 316.23 — Timing Of Requests For Orphan-drug Designation; Designation Of Already Approved Drugs

21 C.F.R. § 316.23

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(a) A sponsor may request orphan-drug designation at any time in its drug development process prior to the time that sponsor submits a marketing application for the drug for the same rare disease or condition.

(b) A sponsor may request orphan-drug designation of an already approved drug for an unapproved use without regard to whether the prior marketing approval was for a rare disease or condition.