Create a Research Consent Form in 30 Seconds
Build a fillable informed-consent form, send it to your participants, and collect signed PDFs.
See a Research Consent Form in action
One prompt in, a finished document out — fully editable and yours to download. Not a template, not a mockup.
From idea to download in three steps
Describe your study, its procedures, and any risks
Send the informed-consent form to your participants
Collect signed, dated research consent PDFs
Everything you need, nothing in the way
Built for speed and polish — so the document is done before you would have finished formatting the first page.
Purpose and Procedures Section
AI drafts a plain-language explanation of the study, what participation involves, and how long it takes — the core of informed consent.
Risks, Benefits, and Confidentiality
Clear sections on potential risks, any benefits, and how participant data will be stored and kept confidential.
Voluntary Participation and Withdrawal
States that participation is voluntary and that participants may withdraw at any time without penalty.
Participant E-Signature
Participants read the form and sign on any device; you collect dated, completed consent PDFs for your records.
Tweak with AI
Refine any result by chatting — "make it warmer", "add my logo top-right", "shorten the intro". The document updates in place.
Print-ready PDF
Export a clean, print-ready PDF, or publish your document as a one-page webpage — ready to send, share, or print.
How to make a research consent form
A research consent form documents a participant's informed consent to take part in a study. Informed means they understood the purpose, the procedures, the risks, and their right to withdraw before they agreed. With EZdoc you describe the study once and get a fillable consent form to send to each participant.
What to include
- The study's purpose and what participation involves
- Potential risks and any benefits
- How participant data is stored and kept confidential
- A statement that participation is voluntary and can be withdrawn
- An acknowledgment line, the date, and a signature
Each section exists so the participant can make a real decision. EZdoc drafts the purpose, risk, confidentiality, and withdrawal language in plain English, then lets you refine it to match your protocol before you share.
Send it and collect the signatures
Share the link with your participants by email or in your recruitment materials. Each person reads the form, fills in their details, and signs in the browser — ideal for remote or online studies. You collect a dated, completed PDF per participant for your study records. Always confirm any IRB or ethics-board wording before you begin.
Questions, answered plainly
What should a research consent form include?
The study's purpose, what participation involves, risks and benefits, confidentiality and data-handling, a statement that participation is voluntary, the date, and a signature.
What makes consent "informed"?
Participants must understand the study, the risks, and their right to withdraw before they agree. EZdoc drafts each of these sections in plain language so consent is genuinely informed.
Can participants sign the consent form online?
Yes. Participants read the form and sign in the browser, and you collect a dated PDF for each one — useful for remote or online studies.
Does this meet IRB requirements?
EZdoc gives you a clear, structured informed-consent document, but always check your institution's IRB or ethics board for any required wording before you collect signatures.
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