FDA Drug Approval: Review Time Has Decreased in Recent Years.

Abstract

New drugs marketed in the United States must be approved first by the Food and Drug Administration (FDA). Approval comes after FDA has determined from data submitted by a drug's sponsor that the drug is safe and effective for use as indicated on its label and that the manufacturer can ensure its quality. Various parties calling for the legislative reform of FDA in recent months are concerned with the length of the approval process. Advocates of reform argue that shortening the time it takes to get new drugs approved will contribute both to public health, by making effective therapies available sooner to people who need them, and to the economic health of the pharmaceutical industry, by allowing drug manufacturers to sell their products sooner. Opposed to major reform, FDA claims that in recent years review time has been reduced considerably.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1995
Accession Number
ADA311544

Entities

Organizations

  • United States Government Accountability Office

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Accounting
  • Coefficients
  • Contrast
  • Drug Users
  • Food Safety
  • Health
  • Human Resources
  • Information Science
  • Intervals
  • Marketing
  • Prescription Drugs
  • Public Health
  • Regression Analysis
  • Statistical Analysis
  • Statistics
  • United Kingdom
  • United States

Fields of Study

  • Medicine

Readers

  • Clinical Trial Research.
  • Economics
  • Educational Psychology