What Is an IRB Service?
IRB services provide comprehensive ethical review and ongoing oversight for research involving human participants. From initial submission through study completion, these services help researchers navigate regulatory requirements, maintain compliance, and ensure the protection of participant rights and welfare throughout the research process. IRB services are suitable for a wide variety of study types, including clinical, behavioral, social, and educational research. They also provide guidance on amendments, annual check-ins, and reporting requirements, making the research process more efficient and helping investigators focus on high-quality study design.
A Quick Guide to IRB Services
An IRB service provides ethical review and oversight for research involving human participants. These services ensure that studies comply with federal regulations and that the rights, safety, and welfare of participants are protected.
IRB services are used by a wide range of researchers and organizations, including academic investigators, independent researchers, sponsors, and companies conducting clinical, social, or behavioral research involving human subjects.
IRB services typically include initial study review, review of amendments or revisions, continuing review (such as annual check-ins), and ongoing support to help researchers maintain compliance throughout the lifecycle of their study.
Most research involving human participants requires IRB review and approval before the study begins, in accordance with regulations from the Office for Human Research Protections and, when applicable, the U.S. Food and Drug Administration.
Why Work with Our IRB Service?
Over a Decade of Trusted IRB Expertise for Your Research Needs
Solutions IRB is your reputable, fast, and friendly IRB service. Here at Solutions IRB, we recognize the importance of a fast, thorough, and ethical IRB review. We work diligently to have quick turnaround times, easy access to our team members, and individualized support for our clients.
As a institutional review board:
- We are an independent IRB, fully accredited by the Association for the Accreditation of Human Research Protection Programs (AAHRPP).
- We specialize in fast and reliable service.
- We provide friendly, knowledgeable and available staff to help you navigate through the process.
Key Benefits of Working with Solutions IRB
- Speed & Efficiency:
We provide quick turnaround times without compromising on quality. IRB ethics review is all we do, so we can focus on ensuring your research receives a top quality review in a timely manner. - Accreditation:
Proudly accredited by AAHRPP, ensuring the highest standards in ethical review. - Professional Team:
Our expert reviewers ensure timely and ethical quality reviews that follow regulations. Our knowledgeable administrative team are available to guide you every step of the way, making the IRB process straightforward. - Affordable Pricing:
Competitive pricing without sacrificing expertise or service. - Expertise in all review levels:
Our team has expertise in all levels of IRB review; from clinical trials to educational studies and everything in between.
Friendly and Easy to Reach Staff
Our expert administrative staff is always available to assist you. When you call, you’ll speak directly with our staff, who are ready to assist you whenever needed. No waiting days for an email response—our team will connect with you through your preferred method of communication within hours. Whether it’s email, phone, Zoom, or instant messaging, we are here to help.
Insights From Solutions IRB:
A Beginner’s Guide to IRB Submission
Submitting your first Institutional Review Board (IRB) application can feel overwhelming. Between preparing your study documents, understanding regulatory requirements, and ensuring everything aligns, it’s easy to wonder where to begin. The good news is that with a little preparation, the process becomes much more manageable. Taking the time to organize your study before submitting it…
What Makes an IRB Application Get Approved Faster?
Submitting an IRB application can feel like a waiting game—but in many cases, delays are preventable. While every study is different, there are several consistent factors that help applications move through the review process more efficiently. One of the most important elements is completeness. Applications that are fully developed at submission—rather than missing documents or…
External vs. Private vs. Central IRBs: What’s the Difference?
When planning a study that involves human participants, one of the first steps is securing approval from an Institutional Review Board (IRB). Researchers often encounter terms like external IRB, central IRB, and private IRB—sometimes even used interchangeably. While these concepts overlap, they are not identical. Understanding the distinctions can help researchers choose the right partner…