Data-driven protocol risk analysis

Risklick uses explainable AI to design and optimize clinical trial protocols based on empirical data. Risklick-AI empowers clinical trial professionals to optimize the medical and operational aspects of any clinical trial protocol before it starts, so you can conduct cheaper, faster, safer trials. Risklick-AI’s multilayer analysis identifies weak points in your proposed study, giving you the information you need, optimize your protocol, avoid delays and prevent deviations.

Risklick-AI optimizes:

  • Eligibility criteria
  • Outcomes
  • Sample size
  • Study duration
  • Readability
  • Safety
  • And other critical quality factors.
We make the risk mitigation process easy for study teams to understand. Our comprehensive and actionable risk analysis report includes corrective measures and suggestions to improve quality. Boost the probability of a successful trial now!