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 IRB and Research Compliance Consulting

We we specialize in providing expert guidance and support for Institutional Review Boards (IRBs), research teams, Principal Investigators and students. Our intent is to assist you in  is to ensuring that your research projects adhere to the highest ethical standards and regulatory requirements, enabling you to focus on what matters most—advancing knowledge and innovation. 


We are experienced professionals, and are dedicated to helping you navigate the complexities of IRB review and approval, research compliance events, and ensuring that your studies are not only compliant but also protect participants.


Features

Expert Guidance

We provide tailored consulting services to navigate the complexities of the IRB submission and review process, as well as research compliance. We can help you ensure that your project meet all regulatory requirements and you are informed of best practices.

Comprehensive Support

From initial protocol planning to IRB submission to study close out, we can offer support to PIs and study teams by reviewing and editing your IRB submissions, or helping you understand the determinations your IRB has made ans what is required of you and your study team. 

Temporary IRB Staffing

We can provide temporary staffing support for IRBs. All consultants are Certified IRB Professionals (CIP).

Regulatory Updates

We can assist you in understanding regulatory updates and changes and best practices in both IRB and research compliance, helping to ensure your organization remains compliant and up-to-date.

About Us

 We specialize in providing expert guidance and support in Institutional Review Board (IRB) processes and research compliance.


We are dedicated to helping researchers navigate the complex landscape of regulatory requirements, ensuring that their studies are conducted ethically and in accordance with federal and institutional standards.


With years of experience in the field, in both Academic and Hospital/Healthcare settings, we are committed to fostering a culture of compliance and integrity in research, empowering our clients to focus on their research.

Frequently Asked Questions

What is an IRB and why is it important?

An Institutional Review Board (IRB) is a committee that reviews and approves research involving human subjects to ensure ethical standards are met. It is crucial for protecting the rights and welfare of participants.

How can your consulting services help my research?

Our consulting services provide guidance on IRB submissions, compliance with federal regulations, institutional policies and best practices for conducting ethical research, ensuring your project meets all necessary standards.


We can assist you with drafting or reviewing any documents that will be submitted to your IRB and can also assist with any determinations or requirements made by your IRB.


What types of research can you support?

We support a wide range of research types, including clinical trials, social and behavioral studies, and educational research.

How long does the IRB review process take?

The IRB review process at your institution can vary in duration depending on the complexity of the study and the completeness of the submission. Typically, it can take anywhere from a couple weeks to several months depending on your proposed research and the quality of your submission.

Let's chat!

Please provide your contact information and a little bit about your study and/or what we may be able to help you with and we will get back to you! Typically you should receive a response within 24 hours.

Contact Us

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