Beginning your first human subjects research study comes with many questions, and understanding the IRB process is an important first step. Our beginner-friendly guides walk you through every step—from planning your study to maintaining approval after your research begins.
Every successful IRB submission starts with a well-designed study. Before you begin the application process, make sure your research question, methodology, and study procedures are clearly defined.
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A qualified research team is essential for conducting ethical research. Understanding each team member’s responsibilities and ensuring the appropriate training is completed helps your study run smoothly and remain compliant.
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Your research protocol serves as the roadmap for your study, outlining your objectives, methodology, participant population, study procedures, and plans for protecting participants. A clear, comprehensive protocol helps the IRB understand your study and provides the foundation for a successful review.
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Participant-facing documents should be clear, accurate, and easy to understand. Writing in plain language helps participants make informed decisions and supports the informed consent process.
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A complete, consistent application helps the IRB understand your study and can reduce requests for revisions. Taking the time to review your documents before submission can save valuable time later.
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Once your application is submitted, the IRB evaluates your study to ensure participant rights and welfare are protected. Knowing what happens during review can help you prepare for a smoother experience.
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Receiving IRB approval is just the beginning. Throughout your study, you’ll need to maintain compliance by reporting changes, submitting required updates, and keeping accurate study records.
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The IRB process doesn’t end with these seven steps. No matter where you are in your research journey, our growing library of educational resources is here to help you navigate the IRB process with confidence. Explore additional articles covering clinical research, social and behavioral research, vulnerable populations, research ethics, and much more.
Ready to Begin Your Research Journey?
From first-time submissions to ongoing research oversight, our knowledgeable team is here to help you navigate the IRB process with confidence. Schedule a meeting to discuss your research, ask questions, and learn how Solutions IRB can support your project from submission through study completion.