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Solutions Evidence Synthesis

Governed evidence synthesis from source material to reusable output

Turn literature, prior documents, reviews, and study artifacts into linked evidence packs and structured summaries without losing source context, review history, or downstream traceability.

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SYNTHESIZE WITH TRACEABILITY

Everything teams need to turn source material into governed evidence

Bring source review, evidence packaging, structured summaries, and reusable rationale into one connected workflow instead of stitching evidence together by hand.

Centralize source material

Keep literature, guidelines, prior submissions, supporting documents, and study artifacts connected inside the same governed workspace.

Generate structured summaries

Produce reusable evidence outputs in formats teams can review, compare, and carry into protocol design, documents, and downstream decisions.

Review before reuse

Put expert validation into the synthesis path so downstream teams inherit reviewed evidence, not rough notes or unsupported summaries.

Preserve the source trail

Keep every evidence output connected to the source material, rationale, review activity, and decisions it supports.

Evidence synthesis workspace preview

Built on trusted standards

Structured around the standards that guide modern clinical development.

Solutions Trial Design

Trial Design runs inside Studio

Plan trial structure, connect evidence, and coordinate governed design work from one shared operating surface.

Model the protocol. Capture trial structure in the same governed surface used by the rest of the team.

Review in context. Keep approvals tied to the design record instead of external spreadsheets and slide decks.

Carry forward decisions. Pass the agreed structure directly into study start-up work without repeated reinterpretation.

Trial design summary preview

Solutions Medical Writing

Medical Writing stays attached to the record

Create, revise, and review controlled clinical content with governed drafting, shared context, and traceable human oversight.

Draft with context. Keep writing workflows connected to the governed source material they depend on.

Control revisions. Move drafts, comments, and approvals through the same visible decision path.

Preserve history. Track how clinical content changed and who approved each step.

Medical writing documents preview

Solutions Scientific Insights

Scientific Insights stays governed in Studio

Use governed AI workflows and connected context to surface scientific insight without losing traceability or review control.

Surface insight with structure. Use governed AI flows to produce outputs that teams can actually evaluate and apply.

Keep operators in control. Make the review path explicit before insight becomes action.

Trace the outcome. Preserve the path from context to insight to decision in one system.

Scientific insights preview

Pricing

Choose the plan that matches your clinical workload

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.

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Ignite

For small teams launching a first trial who need core governance, evidence, and document controls.

€1,500 / month / Billed annually
  • 1 active trial
  • 3 users
  • 500,000 monthly AI tokens
  • Core study workspace
  • Basic governance controls

Accelerate

For teams managing multiple active studies that need more capacity, stronger governance, and faster support.

€4,500 / month / Billed annually
  • 3 active trials
  • 8 users
  • 2,000,000 monthly tokens
  • 15 active rules
  • Persona engagement feedback included
  • Trial feasibility review included

Scale

For enterprise teams running larger study portfolios with custom limits, identity controls, and dedicated support.

€15,000 / month / Billed annually
  • Unlimited active trials
  • Unlimited users
  • 8,000,000 included monthly AI tokens
  • Identity and access controls
  • Dedicated onboarding and support

Get started

See how governed study work fits into your operating model.

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.

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