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Evaluation of Legal Legislation Compliance and Readability of Clinical Trial Informed Consent Forms.

Buket GungorMualla AylinAyse AsenaElif Inci SomuncuogluNihan Burul BozkurtSerife Reyhan UckuAyse Gelal
Published in: Therapeutic innovation & regulatory science (2020)
Results showed that researchers need easy-to-read ICF writing training that fits legal regulations.
Keyphrases
  • clinical trial
  • health information
  • phase ii
  • single molecule
  • study protocol
  • open label
  • double blind
  • randomized controlled trial
  • phase iii
  • healthcare
  • social media