Act of June 25, 1938, ch. V, subch. B, sec. 525 (as amended)
recommendations for investigations of drugs for rare diseases or conditions
recommendations for investigations of drugs for rare diseases or conditions
Sec. 525. [21 U.S.C. 360aa] (a) The sponsor of a drug for a disease or condition which is rare in the States may request the Secretary to provide written recommendations for the nonclinical and clinical investigations which must be conducted with the drug before—
(1) it may be approved for such disease or condition under section 505, or
(2) if the drug is a biological product, it may be licensed for such disease or condition under section 351 of the Public Health Service Act.
If the Secretary has reason to believe that a drug for which a request is made under this section is a drug for a disease or condition which is rare in the States, the Secretary shall provide the person making the request written recommendations for the nonclinical and clinical investigations which the Secretary believes, on the basis of information available to the Secretary at the time of the request under this section, would be necessary for approval of such drug for such disease or condition under section 505 or licensing of such drug for such disease or condition under section 351 of the Public Health Service Act.
(b) The Secretary shall by regulation promulgate procedures for the implementation of subsection (a).
- Cross-references to the US Code
- 21 U.S.C. 360aa
- Public laws referenced
- 97-414107-281