This subpart applies to certain biological products that have been studied for their safety and efficacy in ameliorating or preventing serious or life-threatening conditions caused by exposure to lethal or permanently disabling toxic biological, chemical, radiological, or nuclear substances. This subpart applies only to those biological products for which: Definitive human efficacy studies cannot be conducted because it would be unethical to deliberately expose healthy human volunteers to a lethal or permanently disabling toxic biological, chemical, radiological, or nuclear substance; and field trials to study the product's efficacy after an accidental or hostile exposure have not been feasible. This subpart does not apply to products that can be approved based on efficacy standards described elsewhere in FDA's regulations (e.g., accelerated approval based on surrogate markers or clinical endpoints other than survival or irreversible morbidity), nor does it address the safety evaluation for the products to which it does apply.
21 CFR Part 601 · Licensing
§ 601.90 Scope
Independent copy, not an official legal edition. 21 CFR is a U.S. Government work in the public domain; this text comes from the eCFR and the annual CFR edition, and may lag recent amendments. The authoritative version is on ecfr.gov. Compliome is not affiliated with or endorsed by FDA. Not legal advice.
FDA guidance that cites § 601.90
- Demonstrating Substantial Evidence of Effectiveness for Human Drug and Biological Products: Draft Guidance for Industry draft 24 Jun 2026
- Acute Radiation Syndrome: Developing Drugs for Prevention and Treatment draft 19 Apr 2023
- Mpox: Development of Drugs and Biological Products; Guidance for Industry draft 19 Jan 2023
- Antibacterial Therapies for Patients With an Unmet Medical Need for the Treatment of Serious Bacterial Diseases 2 Aug 2017
- Emergency Use Authorization of Medical Products and Related Authorities: Guidance for Industry and Other Stakeholders 13 Jan 2017
- Product Development Under the Animal Rule 2 Oct 2015
- Neglected Tropical Diseases of the Developing World: Developing Drugs for Treatment or Prevention 7 Jul 2014
Amendment history
Federal Register documents that created or amended this section.
- 38 FR 32052 20 Nov 1973