RapidIRB
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FAQ

About Rapid IRB

Rapid IRB is a streamlined, independent IRB service that uses a smart algorithm to provide instant exemption or quality improvement determinations for low-risk research. We specialize in fast reviews for minimal-risk studies.
For qualifying studies, the system instantly generates your official determination letter, usually within seconds of submission.
None. You only need to enter the study title, the names of investigators (same facility), and a basic description of the study plan.
You will be notified immediately. Studies that exceed minimal risk or don’t meet criteria will need to be submitted to a full IRB. (We may recommend partners.)

Exempt Determination: $199

QIPR Review: $75

Both include official determination letters.

Yes. We are registered with the Office for Human Research Protections (OHRP) and hold Federal wide Assurance (FWA).
Yes. Each site must obtain a separate determination letter and designate a Site PI. Up to five additional investigators can be listed per site.
Yes. Optional support is available to help you prepare your submission, email us for consultation.

Email us at support@rapidirb.com or use the contact form

About Our Exempt Determination Tool

Typical examples include:

  • Educational practices
  • Operational and program evaluations
  • Retrospective chart reviews
  • Survey/interview studies with adults
  • Secondary data analysis with de-identified datasets
Our submission portal guides you through a decision tree aligned with federal exemption criteria. If your project meets requirements, a determination letter is automatically generated.
Minor changes likely won’t affect exemption status. For major changes (e.g., to population, risk, or study design), email us for a review. Responses take 3–5 business days.
Yes. Many journals accept exempt studies. Your determination letter from Rapid IRB serves as valid documentation.
You may not need Rapid IRB, but we can provide an independent exemption letter if required by sponsors, collaborators, or journals.

Informed consent ensures that all research participants are fully informed about the requirements, risks, benefits, and alternatives before they decide to participate.

About Our QIPR Tool

Our Quality Improvement/Not Human Subjects Research (QI/NHSR) tool evaluates QI projects to determine eligibility for a non-IRB QIPR determination letter.
Common examples include workflow improvements, program evaluations, and internal quality initiatives that don’t involve human subject research.

If eligible, your QIPR determination letter is automatically generated and available for immediate download.

Yes. Many journals accept QI studies with appropriate documentation, which we provide.
We can still provide an independent QIPR letter if needed for collaboration or publication.

Powerful Tools for Research Compliance

Our comprehensive suite of tools helps you navigate the complex landscape of research ethics and regulatory compliance for low-risk studies.

QIPR Tool

Determine if your project qualifies as Quality Improvement

Get an instant determination for your Quality Improvement and Practice-based Research projects with our expert-designed assessment tool.

Get QIPR Determination $79

Exempt Determination Tool

Check if your research qualifies for exempt status

Receive an instantaneous and valid exempt determination under federal regulations for low-risk research studies.

Get Exempt Status $199

Got more questions?

If you have any questions or need assistance, please reach out to us at support@rapidirb.com for prompt support and guidance.

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Choose the Tool for Your Research Project

Get started with instant IRB determinations

QIPR Tool

$79 one-time payment

Perfect for Quality Improvement and Practice-based Research projects

  • Instant QIPR determination
  • Expert-designed assessment
  • Retain full research rights
  • Compliance documentation
Get QIPR Tool - $79
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Exempt Determination Tool

$199 one-time payment

Ideal for low-risk research studies requiring exempt status

  • Instant exempt determination
  • Federal regulation compliance
  • Valid IRB documentation
  • Retain full research rights
Get Exempt Tool - $199

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