Track and verify clinical trial patient consent forms automatically

Automatically captures, verifies, and logs clinical trial consent forms, then flags any that are missing or expiring.

How the work actually flows

It branches. Every path runs.

Pattern: Parallel Split (2) ยท Transient Trigger (23)

flowchart TD trig>"participant submits consent form"]:::trig s0["verify form completeness"]:::task s1["claude reviews against guidelines"]:::svc s2[("log with audit trail")]:::store trig --> s0 s0 --> s1 s1 --> s2 gx{"+ who gets notified"}:::gate s2 --> gx p00["send confirmation email"]:::task gx -->|"email investigator"| p00 p10["send confirmation email"]:::task gx -->|"email participant"| p10 p00 --> out p10 --> out out[/"audit ready consent record logged"/]:::out pay{{"stays compliant without manual chasing"}}:::pay out --> pay s1 -. "failures recorded, run continues" .-> out classDef task fill:#e7f6fe,stroke:#34b8f0,color:#2c2a29 classDef svc fill:#f6f8fa,stroke:#7c8795,color:#2c2a29 classDef mi fill:#e7f6fe,stroke:#0079a8,color:#2c2a29,stroke-width:2px classDef human fill:#fff,stroke:#0079a8,color:#0079a8 classDef store fill:#f6f8fa,stroke:#0079a8,color:#2c2a29 classDef trig fill:#00a4eb,stroke:#0079a8,color:#fff,font-weight:bold classDef trigtime fill:#00a4eb,stroke:#0079a8,color:#fff,font-weight:bold classDef trigdata fill:#8ad4f5,stroke:#0079a8,color:#06314c,font-weight:bold classDef gate fill:#fff,stroke:#e8a23d,color:#6b4708,font-weight:bold classDef out fill:#1f9d6b,stroke:#167a53,color:#fff,font-weight:bold classDef pay fill:#06314c,stroke:#021f33,color:#fff
Starts itA stepAn outside serviceA record or sheetEvery pathResultPayoff
Build size
Advanced

A larger build with multiple systems, AI reasoning, and custom rules.

Business functions
AI Agents & Autonomous SystemsEmail AutomationSpreadsheet & Database OpsAPI & Webhook IntegrationSecurity & Compliance
Connects
ClaudeGoogle SheetsGmail
Featured in

The problem it solves

Chasing down paper or scattered digital consent forms and manually checking each one against strict regulatory rules is slow and risky. A single missed or incomplete form can put a trial's compliance at risk.

Who it fits

Clinical trial sponsors, CROs, or research sites running patient consent programs.

How it works

  1. A participant submits a signed consent form through the portal
  2. The system timestamps it and checks that every required field is complete
  3. Claude reviews the form against clinical trial guidelines
  4. The record is logged with a full audit trail, and the investigator and participant get a confirmation email
  5. Each day, the system checks for consents that are missing or about to expire
What you get

Consent forms that never slip through the cracks

Every patient consent form gets captured, checked, and logged automatically, with alerts before anything expires or goes missing.

What you get

An audit-ready consent record for every submission, plus a daily compliance report flagging missing or expiring consents.

What you need

An Anthropic API key, a Google Sheets account, and an email account for notifications.

We can build this. But should you?

The hard question is not how to build it. It is whether this is the right thing to build first.

That is what a Fractional Chief AI Officer figures out with you, before anyone writes a line of code.

Let's Talk Strategy

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