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.