Research Tool

IRB Proposal Generator

Choose an output format, fill in your study details, and select the measures you will administer. The tool assembles a structured document — either a generic human-subjects protocol, an academic medical center consent form, or a university IRB review form — that you can download as Markdown or PDF. Standard institutional language is included as clearly marked, editable template text; anything you leave blank is flagged as “[to be completed]” rather than invented. It is a starting template; review and adapt it to your institution's IRB requirements before submission.

Output format

Study details

Investigator contact (consent & review forms)

University review form — submission details

Used only for the university IRB review form.

Study narrative

Measures

Risks, benefits & protections

Medical consent form — additional fields

Used only for the academic medical center consent form.

HIPAA authorization

University review form — additional fields

Used only for the university IRB review form.

Screening questions

A study title and principal investigator are the minimum needed to assemble a document; every other field falls back to a “[to be completed]” marker you can edit afterwards.