Pharmaceutical Companies

Standardize trial decisions across global programs

Clinical development, data management, operations and IT leaders can govern one reusable trial definition across functions. Teams retain local rationale while standards and downstream interfaces stay controlled.

Therapeutic Area Heads

Own clinical strategy and approve trial designs across a therapeutic or disease area.

Global Data Management Heads

Govern data standards, collection and management across trials and downstream systems.

Global Clinical Operations Heads

Set the operating model for trial planning, contracting, start-up and execution.

R&D IT Leads

Own the target architecture, technology roadmap, security posture and implementation resources.

Use casesScientific design

Turn scientific intent into a governed trial definition

Clinical scientists and trial designers structure objectives, endpoints, eligibility, interventions and the SoA in one current definition. Reviewers can trace rationale and changes before downstream work begins.

Structure the design. Capture objectives, endpoints, eligibility, interventions and activities as connected trial elements.

Reuse prior decisions. Bring forward approved patterns without losing the evidence and rationale behind them.

Review before handoff. Resolve ambiguity while the scientific and operational owners can still change the design.

                    flowchart TD
  A["Scientific intent"] --> B["Structured trial design"]
  B --> C["Cross-functional review"]
  C --> D["Approved definition"]

Use casesData acquisition

Prepare data acquisition from the digital protocol

Clinical data managers review the SoA, biomedical concepts and data requirements before eCRF and EDC configuration. Target-specific automation still depends on mappings, integration, validation and human approval.

Review data requirements early. Connect activities, assessments and data elements before the build is locked.

Prepare the handoff. Package governed inputs, mappings and target findings for downstream configuration.

Keep approval explicit. Retain UAT, validation and data-management accountability at the receiving boundary.

                    flowchart TD
  A["Digital protocol and SoA"] --> B["Data requirements"]
  B --> C["Acquisition package"]
  C --> D["EDC or eCRF build review"]

Use casesTechnology integration

Connect downstream systems to one governed definition

R&D IT leaders and technical experts can evaluate a versioned source for APIs, mappings and system handoffs. The target architecture remains a customer decision rather than a prescribed platform pattern.

Map the ecosystem. Identify authoritative boundaries, consumers and duplicate entry before choosing an integration pattern.

Define the interface. Make versions, mappings, errors and amendment behavior explicit for each consumer.

Plan the operating model. Include security, validation, observability, support and upgrade ownership in the implementation.

                    flowchart TD
  A["Governed trial definition"] --> B["Versioned API or export"]
  B --> C["Mapping and validation"]
  C --> D["Downstream consumer"]

Built on established clinical standards

TrialStack's canonical model gives teams and agents one governed trial definition that supports structured exports to downstream systems.

Customers

Compare clinical operating models

See how sponsors, CROs, trial units and research sites use the same governed trial definition for different workflows.

Contract Research Organizations

Give sponsor-facing delivery teams one governed trial definition for protocol authoring, data acquisition preparation and start-up.

Biotechnology Companies

Give a lean development team one governed trial definition for scientific design, protocol authoring and data acquisition preparation.

Clinical Trial Units

Connect investigator intent, protocol authoring and operational preparation across scientific and delivery teams.

Academic Medical Centers

Connect investigator-led design, protocol authoring and trial start-up across academic departments.

Research Sites

Carry sponsor intent into site start-up, data acquisition and amendment review without losing context.

Pricing

Choose capacity for the trials you run

Every plan includes TrialStack Studio for governed trial design, evidence and document authoring. Plans differ by active trials, seats, AI usage and concurrent runs.

Ignite

For biotechnology teams and research sites preparing their first active trial. Replace disconnected documents and handoffs with one governed workflow.

$750/ month

Free Trial

1 active trial
3 seats included; add more at $100 / month
500,000 monthly AI tokens
2 concurrent AI workflows

Accelerate

For CRO and pharmaceutical teams coordinating up to three active trials. Keep design, evidence and review aligned across parallel work.

$3,000/ month

Free Trial

3 active trials
8 seats included; add more at $100 / month
2,000,000 monthly AI tokens
5 concurrent AI workflows

Scale

For sponsors, trial units and academic medical centers managing portfolios. Standardize governed trial workflows across departments and up to 20 active trials.

$3,750/ month

Free Trial

20 active trials
15 seats included; add more at $100 / month
8,000,000 monthly AI tokens
10 concurrent AI workflows

Get started

Give your next clinical trial a governed foundation

Keep protocol decisions, document authoring and data acquisition aligned around one trial definition. Try TrialStack Studio free for 3 days.

Free Trial Explore Studio