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Solutions Scientific Insights

Governed scientific insight from study context to decision-ready output

Ask questions across evidence, study records, documents, and workflow history while keeping answers connected to source context, human review, attribution, and follow-through.

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ASK WITH TRACEABILITY

Everything teams need to turn study signals into governed insight

Surface scientific signals, compare context, and generate reusable outputs from connected study records instead of relying on isolated prompts, pasted context, and unsupported answers.

Ask across live context

Run insight workflows across connected study records, evidence, documents, comments, and decisions without manually rebuilding the context.

Keep review in the loop

Make human review and approval part of the workflow so generated insight stays attributable, controlled, and fit for use.

Turn prompts into workflows

Convert repeated scientific questions into shared flows teams can reuse consistently across studies.

Preserve the decision path

Keep the trail from source context to generated insight to downstream action visible after the output is created.

Scientific insights-style 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 Evidence Synthesis

Evidence Synthesis keeps source and output connected

Synthesize source material into governed summaries, linked evidence artifacts, and reusable workflows for trial planning.

Route source material. Bring documents, notes, and findings into a single synthesis workflow.

Generate linked artifacts. Keep summaries and evidence outputs attached to their underlying source set.

Reuse the workflow. Apply the same governed synthesis pattern across studies without rebuilding the process.

Evidence synthesis 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.

Explore Tiers

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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