Turn sponsor protocols into work your site can execute.

Generate practical visit and screening documents from the approved protocol, keep them current after amendments, and reduce the overhead of onboarding each new study.

Start studies with less manual setup

Generate visit worksheets and eligibility screening forms directly from the protocol.

Give staff clear instructions

Translate dense protocol requirements into visit-level operational tools.

Increase site capacity

Standardize repeatable start-up work so the team can support more studies.

Choose your role

What are you responsible for?

Choose the closest role. Each view focuses on the work, risk, and outcome that role owns.

Clinical Research Coordinator Generate accurate visit worksheets and eligibility screening forms from the protocol, save setup time, and stay aligned after amendments. See my Trelice view → Principal Investigator Understand and oversee a new clinical study faster, verify visit requirements, and take on studies with less operational overhead. See my Trelice view → Site Director / Owner Activate studies faster, standardize coordinator workflows, increase staff capacity, and take on more studies without proportional overhead. See my Trelice view →

None of these quite fit? The demo can be shaped around your workflow.

Tell us what you own →

See one approved protocol become the documents your team needs.

Bring a synopsis or protocol. We'll show the workflow using the work your organization already does.

Book a tailored demo →