Code of Federal Regulations (alpha)

CFR /  Title 21  /  Part 316  /  Sec. 316.23 Timing of requests for orphan-drug designation; designation

(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. [78 FR 35133, June 12, 2013]