IRB Advisors offer consulting service to researchers and students who may need assistance with IRB submission and approval, clinical research support services, IND support, monitoring, auditing, IRB/HRPP consulting and educational services to contract research organizations, independent researchers and those responsible for the oversight of research with human participants.  Our well qualified consultants include auditors, clinical research associates/monitors, regulatory attorney, clinical research coordinators, project managers that offer expert personalized service that is reliable and compliant with federal regulations that govern research.


We offer on-call regulatory review and support services to individual investigators, large or small organizations. Our well qualified consultants can assist with attaining IRB approval for exemptions, expedited review, full-Board and more. 


Read More


Clinical          Research


We provide consultation on all aspects of IRB and Human Research Protection Programs operations. Our highly experienced consultants can guide you through program development, temporary staffing among other regulatory functions.


 Read More


Project Management


Read More



We create specialized human research training and education programs. Our services can be tailored to meet your needs through our certification program, institutional training programs and one on one sessions critical to human subject's protections.


Read More


IND                  Support












Contact Us: 

Phone: (347)671-9867