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Turn regulatory complexity into Turn regulatory complexity into clarity

AI tools that follow submissions, timelines and compliance.

Site Activation Checklist RunnerVisit Schedule & Reminder HelperPatient Diary & PRO Summary ToolDeviation & Query Triage CompanionRegulatory Doc Assembly HelperAdverse Event Monitor Site Activation Checklist RunnerVisit Schedule & Reminder HelperPatient Diary & PRO Summary ToolDeviation & Query Triage CompanionRegulatory Doc Assembly HelperAdverse Event Monitor

How you can work with us

Choose the path that fits your needs

Self-Serve

Triform Platform

Build and deploy your own automations with our intuitive platform.

  • No coding required
  • Instant deployment
  • Pay as you grow
Open App
Enterprise

Triform Services

Let our experts build, deploy, and maintain your automations for you.

  • Custom integrations
  • SLA guarantees
  • Dedicated support
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Why Pharma needs automation

$8M
Tufts CSDD

lost revenue per day for a delayed drug launch

What we can build for you

Sample automations we can build for you and your organization

Contract Review Queue Management

Centralize all contract review requests, auto-classify by type and priority, extract key terms with AI, and route to the right reviewer. Give legal complete visibility into their queue.

Trigger
Request Submitted API
Related
Legal & Compliance Slack
View use case →

How it works

From discovery to deployment

01

Free - Discovery & scoping

We review your study protocols, site management workflows, and data collection plans. We identify the manual bottlenecks that extend timelines and increase costs.

Why Partner with Triform?

Speed to Value

Launch in weeks, not months. Our platform accelerates development.

Enterprise Grade

Security, scalability, and reliability built in from day one.

Future Proof

Adapt easily as your business grows and technology evolves.

FAQ

Is this HIPAA and GDPR compliant?

Yes, our platform is designed with privacy-first architecture to meet global health data regulations. We sign BAAs and DPAs and ensure data residency compliance.

Do you support 21 CFR Part 11?

Yes. We provide the necessary audit trails, e-signatures, and security controls to support Part 11 compliance for validated workflows.

Can you integrate with EDC systems like Rave or Veeva?

Yes, we can connect to major EDC and CTMS platforms to automate data flow, query management, and document filing.

Is validation required?

For GxP workflows, yes. We support the validation process with documentation (IQ/OQ/PQ) and controlled release cycles.

Can it handle multi-country trials?

Yes. The platform supports multiple languages and time zones, allowing you to run global studies on a single unified system.

What about patient consent?

We can integrate with eConsent platforms or manage consent tracking to ensure no data is processed without valid patient authorization.

Tell us what you want to automate

Book a call with our team to discuss your process, or describe what you're looking to automate and we'll reach out with next steps.