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Clinical Trial Electronic Portals for Expedited Safety Reporting: Recommendations from the Clinical Trials Transformation Initiative Investigational New Drug Safety Advancement Project.

Raymond P PerezShanda R FinniganKrupa PatelShanell WhitneyAnnemarie Forrest
Published in: JMIR cancer (2016)
Results indicate that an ideal system for sharing expedited IND safety information is through a central portal used by all sponsors. Until this is feasible, electronic reporting portals should at least have consistent functionality. CTTI has issued recommendations to improve the quality and use of electronic portals.
Keyphrases
  • clinical trial
  • quality improvement
  • phase ii
  • adverse drug
  • health information
  • open label
  • social media
  • randomized controlled trial
  • emergency department
  • study protocol
  • clinical practice
  • placebo controlled