US Code
Part A— Drugs and Devices
§ 356c–1. Annual reporting on drug shortages

(a) Annual reports to CongressNot later than March 31 of each calendar year, the Secretary shall submit to the Committee on Energy and Commerce of the House of Representatives and the Committee on Health, Education, Labor, and Pensions of the Senate a report, with respect to the preceding calendar year, on drug shortages that—(1) specifies the number of manufacturers that submitted a notification to the Secretary under section 356c(a) of this title during such calendar year;
(2) describes the communication between the field investigators of the Food and Drug Administration and the staff of the Center for Drug Evaluation and Research’s Office of Compliance and Drug Shortage Program, including the Food and Drug Administration’s procedures for enabling and ensuring such communication;
(3) describes the coordination and alignment activities undertaken pursuant to section 356d(g) of this title;
(4) provides the number of reports that were required under section 374(b)(2) of this title to be sent to the appropriate offices of the Food and Drug Administration with expertise regarding drug shortages, and the number of such reports that were sent;
(5)(A) lists the major actions taken by the Secretary to prevent or mitigate the drug shortages described in paragraph (9);
(B) in the list under subparagraph (A), includes—(i) the number of applications and supplements for which the Secretary expedited review under section 356c(g)(1) of this title during such calendar year; and
(ii) the number of establishment inspections or reinspections that the Secretary expedited under section 356c(g)(2) of this title during such calendar year;
(6) describes the coordination between the Food and Drug Administration and the Drug Enforcement Administration on efforts to prevent or alleviate drug shortages;
(7) identifies the number of and describes the instances in which the Food and Drug Administration exercised regulatory flexibility and discretion to prevent or alleviate a drug shortage;
(8) lists the names of manufacturers that were issued letters under section 356c(f) of this title; and
(9) specifies the number of drug shortages occurring during such calendar year, as identified by the Secretary.
(b) Trend analysisThe Secretary is authorized to retain a third party to conduct a study, if the Secretary believes such a study would help clarify the causes, trends, or solutions related to drug shortages.
(c) DefinitionIn this section, the term “drug shortage” or “shortage” has the meaning given such term in section 356c of this title.

Structure US Code

US Code

Title 21— FOOD AND DRUGS

CHAPTER 9— FEDERAL FOOD, DRUG, AND COSMETIC ACT

SUBCHAPTER V— DRUGS AND DEVICES

Part A— Drugs and Devices

§ 351. Adulterated drugs and devices

§ 352. Misbranded drugs and devices

§ 353. Exemptions and consideration for certain drugs, devices, and biological products

§ 353a. Pharmacy compounding

§ 353a–1. Enhanced communication

§ 353b. Outsourcing facilities

§ 353c. Prereview of television advertisements

§ 353d. Process to update labeling for certain generic drugs

§ 354. Veterinary feed directive drugs

§ 355. New drugs

§ 355–1. Risk evaluation and mitigation strategies

§ 355–2. Actions for delays of generic drugs and biosimilar biological products

§ 355a. Pediatric studies of drugs

§ 355b. Adverse-event reporting

§ 355c. Research into pediatric uses for drugs and biological products

§ 355c–1. Report

§ 355d. Internal committee for review of pediatric plans, assessments, deferrals, deferral extensions, and waivers

§ 355e. Pharmaceutical security

§ 355f. Extension of exclusivity period for new qualified infectious disease products

§ 355g. Utilizing real world evidence

§ 355h. Regulation of certain nonprescription drugs that are marketed without an approved drug application

§ 356. Expedited approval of drugs for serious or life-threatening diseases or conditions

§ 356–1. Accelerated approval of priority countermeasures

§ 356–2. Accelerated approval Council

§ 356a. Manufacturing changes

§ 356b. Reports of postmarketing studies

§ 356c. Discontinuance or interruption in the production of life-saving drugs

§ 356c–1. Annual reporting on drug shortages

§ 356d. Coordination; task force and strategic plan

§ 356e. Drug shortage list

§ 356f. Hospital repackaging of drugs in shortage

§ 356g. Standards for regenerative medicine and regenerative advanced therapies

§ 356h. Competitive generic therapies

§ 356i. Prompt reports of marketing status

§ 356j. Discontinuance or interruption in the production of medical devices

§ 356k. Platform technologies

§ 356l. Advanced manufacturing technologies designation program

§ 357. Qualification of drug development tools

§ 358. Authority to designate official names

§ 359. Nonapplicability of subchapter to cosmetics

§ 360. Registration of producers of drugs or devices

§ 360a. Clinical trial guidance for antibiotic drugs

§ 360a–1. Clinical trials

§ 360a–2. Susceptibility test interpretive criteria for microorganisms

§ 360b. New animal drugs

§ 360b–1. Priority zoonotic animal drugs

§ 360c. Classification of devices intended for human use

§ 360c–1. Reporting

§ 360d. Performance standards

§ 360e. Premarket approval

§ 360e–1. Pediatric uses of devices

§ 360e–3. Breakthrough devices

§ 360e–4. Predetermined change control plans for devices

§ 360f. Banned devices

§ 360g. Judicial review

§ 360g–1. Agency documentation and review of significant decisions regarding devices

§ 360g–2. Third party data transparency

§ 360h. Notification and other remedies

§ 360h–1. Program to improve the device recall system

§ 360i. Records and reports on devices

§ 360j. General provisions respecting control of devices intended for human use

§ 360k. State and local requirements respecting devices

§ 360l. Postmarket surveillance

§ 360m. Accredited persons

§ 360n. Priority review to encourage treatments for tropical diseases

§ 360n–1. Priority review for qualified infectious disease products

§ 360n–2. Ensuring cybersecurity of devices