Research Study Consent Form Template
Create a comprehensive Research Study Consent Form with our AI-powered form builder. Ensure ethical research practices, obtain valid informed consent, and enhance compliance with institutional review boards and regulations. Perfect for academic, clinical, and organizational research projects.
How it works
How it works
How it works
Discover the power of conversational forms generated by Nolana and learn how to get started in few easy steps
Discover the power of conversational forms generated by Nolana and learn how to get started in few easy steps
Discover the power of conversational forms generated by Nolana and learn how to get started in few easy steps
1
Customize the Consent Details
Use our AI form builder to personalize the consent form by entering your study’s specific details, including objectives, procedures, and expected risks and benefits.
2
Share the Consent Form with Participants
Easily distribute the digital consent form via email, secure link, or embedded on your research website to collect responses efficiently from participants.
3
Collect and Store Informed Consents
Safely gather, track, and export completed consent forms for ethical documentation and compliance, ready for review by institutional boards or during audits.
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Nolana
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Forms like these, and many were created in miniutes with Nolana’s powerful AI forms builder - trusted for education, recruitment, and internal ops workflows.
Forms like these, and many were created in miniutes with Nolana’s powerful AI forms builder - trusted for education, recruitment, and internal ops workflows.
Forms like these, and many were created in miniutes with Nolana’s powerful AI forms builder - trusted for education, recruitment, and internal ops workflows.
Other use cases
Other use cases
Research Subject Consent Form Template
Research Subject Consent Form Template
A Research Subject Consent Form is essential for obtaining informed and voluntary agreement from participants before involving them in research. This form helps ensure ethical compliance and participant understanding of the study's nature, risks, and benefits.
A Research Subject Consent Form is essential for obtaining informed and voluntary agreement from participants before involving them in research. This form helps ensure ethical compliance and participant understanding of the study's nature, risks, and benefits.
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User Research Participant Screener Form Template
User Research Participant Screener Form Template
This User Research Participant Screener form is designed to help you quickly identify and qualify suitable participants for your user research studies. Use this AI-generated screener to efficiently filter potential candidates based on your project’s specific criteria, ensuring you recruit participants who best meet your research needs.
This User Research Participant Screener form is designed to help you quickly identify and qualify suitable participants for your user research studies. Use this AI-generated screener to efficiently filter potential candidates based on your project’s specific criteria, ensuring you recruit participants who best meet your research needs.
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Consent to Treatment Form: Downloadable Template & Example
Consent to Treatment Form: Downloadable Template & Example
This Consent to Treatment Form is designed to obtain informed consent from patients or clients before administering medical procedures or treatments. It ensures the individual understands the nature, benefits, risks, and alternatives of the proposed treatment, fostering transparency and ethical care practices.
This Consent to Treatment Form is designed to obtain informed consent from patients or clients before administering medical procedures or treatments. It ensures the individual understands the nature, benefits, risks, and alternatives of the proposed treatment, fostering transparency and ethical care practices.
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AI-Powered Clinical Trial Application Form Template
AI-Powered Clinical Trial Application Form Template
The Clinical Trial Application form is designed to streamline the process of gathering essential information about prospective clinical trials. It ensures all regulatory and ethical requirements are met, collecting critical data about the study, investigators, participants, and protocols.
The Clinical Trial Application form is designed to streamline the process of gathering essential information about prospective clinical trials. It ensures all regulatory and ethical requirements are met, collecting critical data about the study, investigators, participants, and protocols.
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What is Nolana?
Is Nolana free to use?
Who is Nolana for?
How does Nolana work?
What kinds of tasks can Nolana handle?
Can I customise what the AI agents do?
Do you train any models on my data?
Is Nolana secure?
Is Nolana SOC 2 compliant?
What is Nolana?
Is Nolana free to use?
Who is Nolana for?
How does Nolana work?
What kinds of tasks can Nolana handle?
Can I customise what the AI agents do?
Do you train any models on my data?
Is Nolana secure?
Is Nolana SOC 2 compliant?
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Get started for free
Create your first form in seconds and share it with your audience - no credit card required.
Create your first form in seconds and share it with your audience - no credit card required.
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Leroy House, Unit G01, 436 Essex Rd, London N1 3QP
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© 2025 Nolana Limited. All rights reserved.
Leroy House, Unit G01, 436 Essex Rd, London N1 3QP
Want early access?
© 2025 Nolana Limited. All rights reserved.
Leroy House, Unit G01, 436 Essex Rd, London N1 3QP
Want early access?
© 2025 Nolana Limited. All rights reserved.
Leroy House, Unit G01, 436 Essex Rd, London N1 3QP