Model the protocol
Define objectives, endpoints, eligibility, SoA, assessments, risks, controls, and assumptions as structured study decisions.
Solutions Trial Design
Shape protocol structure, evidence, rationale, and operational handoff in one governed workflow instead of rebuilding context across decks, trackers, and disconnected documents.
DESIGN IN ONE GOVERNED FLOW
Keep protocol structure, design rationale, evidence, review, and downstream handoff attached to the same study record from first concept through start-up.
Define objectives, endpoints, eligibility, SoA, assessments, risks, controls, and assumptions as structured study decisions.
Keep comments, approvals, and design trade-offs tied to the actual study record instead of separate decks and spreadsheets.
Push approved design structure into evidence packs, documents, start-up planning, and downstream workflows.
Maintain a visible history of evidence, assumptions, changes, and decisions across the trial lifecycle.
Built on trusted standards
Structured around the standards that guide modern clinical development.
Pricing
Start with one active trial, then scale into multiple studies, larger teams, higher AI usage, stronger governance controls, and priority support as your study-startup work grows.
Ignite
For small teams launching a first trial who need core governance, evidence, and document controls.
Accelerate
For teams managing multiple active studies that need more capacity, stronger governance, and faster support.
Scale
For enterprise teams running larger study portfolios with custom limits, identity controls, and dedicated support.
Get started
Talk through your trial design, evidence review, document generation, and start-up workflows, then choose the Studio, Loop, or Catalyst path that fits your team.