Login / Signup

Ensuring Transparency and Quality of Clinical Trial Reporting in Clinical Pharmacology & Therapeutics: Prospective Trial Registration and Compliance with Reporting Guidelines Are Required for all Clinical Trials.

D Max SmithIris K MinichmayrJoseph F StandingKathleen M GiacominiPiet H van der GraafRichard Wilson Peck
Published in: Clinical pharmacology and therapeutics (2023)
Keyphrases
  • clinical trial
  • phase ii
  • phase iii
  • adverse drug
  • study protocol
  • open label
  • double blind
  • small molecule
  • clinical practice
  • randomized controlled trial
  • quality improvement
  • electronic health record