Study start-up software

Clinical trial study start-up software for research sites.

Move a study from feasibility to activation in one system, starting with the sponsor's statement of work and carrying through to the protocol, sites and regulatory binder.

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What it does

From opportunity to activated study.

Feasibility pipeline

Track each opportunity by stage, with sponsor details, projected subjects, outreach notes and the attached statement of work.

Award and provision

Create the study, its site links, a draft schedule of activities, a start-up checklist and an eISF marker in one step.

Protocol setup

Manage protocols, studies and sites in one hierarchy, with protocol-level approvals that carry down to each site.

Readiness tracking

Tick off the 8-item start-up checklist, and see whether approvals show a site as ready to enroll or blocked.

What is study start-up?

Study start-up is the work between a site being considered for a trial and being ready to enroll. It usually includes feasibility, a qualification visit, contract and budget negotiation, IRB approval, regulatory documents, staff training and a site initiation visit.

Why start-up is hard for small teams

Start-up tasks often run in parallel across inboxes, spreadsheets and paper. Keeping them with the study gives everyone one list, and everything you've set up is already in place when the first subject arrives.

Let's talk about your research projects.

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