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Drug Approval

"Drug Approval" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

expand / collapse MeSH information
Process that is gone through in order for a drug to receive approval by a government regulatory agency. This includes any required pre-clinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance of the drug.


expand / collapse Publications
This graph shows the total number of publications written about "Drug Approval" by people in this website by year, and whether "Drug Approval" was a major or minor topic of these publications.
Below are the most recent publications written about "Drug Approval" by people in Profiles.
  1. Physician-Patient Communication about Novel Drugs and High-Risk Medical Devices. Med Decis Making. 2025 02; 45(2):156-167.
    View in: PubMed
  2. Strength of clinical evidence supporting the United States Food and Drug Administration Accelerated Approvals from 2015 to 2022. BMC Med. 2024 Dec 18; 22(1):587.
    View in: PubMed
  3. Magnitude of effect of low dose colchicine, a newly food and drug administration approved treatment for stroke prevention. J Stroke Cerebrovasc Dis. 2025 Feb; 34(2):108186.
    View in: PubMed
  4. Fear of missing out: Drug availability in the United States vs Canada. J Manag Care Spec Pharm. 2024 Dec; 30(12):1349-1354.
    View in: PubMed
  5. Spending on anticancer drugs among Medicare beneficiaries: Analyzing predictors of drug expenditures. J Cancer Policy. 2024 Dec; 42:100509.
    View in: PubMed
  6. Benefits and risks of FDA-approved amyloid-targeting antibodies for treatment of early Alzheimer's disease: Navigating clinician-patient engagement. Alzheimers Dement. 2024 Nov; 20(11):8162-8171.
    View in: PubMed
  7. Is Canada Moving towards a More Agile Regulatory Approval and Reimbursement Process with a Shifting Role for Real-World Evidence (RWE) for Oncology Drugs? Curr Oncol. 2024 09 18; 31(9):5599-5607.
    View in: PubMed
  8. Postrecurrence Treatment in Neoadjuvant or Adjuvant FDA Registration Trials: A Systematic Review. JAMA Oncol. 2024 Aug 01; 10(8):1055-1059.
    View in: PubMed
  9. Brief of over 300 reproductive health researchers as Amici Curiae in FDA v. Alliance for Hippocratic Medicine. Perspect Sex Reprod Health. 2024 Dec; 56(4):320-328.
    View in: PubMed
  10. The landscape of checkpoint inhibitors in oncology. Eur J Cancer. 2024 Sep; 209:114240.
    View in: PubMed