Know where your sites' staff will struggle on your protocol, before activation.

CRLN turns a study's protocol into realistic decision scenarios for each site role, so sponsors and CROs see readiness before activation.

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What you get

  • Practice scenarios for your protocol. Realistic decisions for each site role on your study: coordinator, investigator, pharmacist, and others.
  • A risk map. The decisions most likely to go wrong on your study, by role and by visit.
  • A readiness report before activation. Reported at group level. Groups of fewer than five people are never shown.
  • Free practice for your sites. Your sites can practice on the scenarios for free. Site staff never pay.

How an engagement works

  • Share the study. Send the public registry record or, under a confidentiality agreement, the protocol.
  • Receive the scenarios and risk map. We deliver the practice scenarios for each site role and the risk map for your study.
  • Sites practice, you get the report. Site staff practice, and you receive the readiness report.

Built to be checked

  • Scored against our own open standard, built on ICH E6(R3).
  • Built with fictional participants. No patient data is used.