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Regulatory compliance and readability of informed consent forms in industry-sponsored drug development clinical trials.

Nahathai DukaewMingkwan Na TakuathungWannachai SakuludomkanKanyarat ChairaksaPreeyaporn KlinjanNimit MorakoteNut Koonrungsesomboon
Published in: Clinical trials (London, England) (2023)
The informed consent forms in industry-sponsored drug development clinical trials were long but incomplete. Our findings draw attention to ongoing challenges in industry-sponsored drug development clinical trials, where deficient informed consent form quality continues to exist.
Keyphrases
  • clinical trial
  • phase ii
  • working memory
  • open label
  • transcription factor
  • phase iii
  • double blind
  • health information
  • healthcare
  • randomized controlled trial