Our Legacy and Reputation
Schulman Associates IRB was founded in 1983 in Cincinnati, OH. In establishing Schulman, founders Alan Schulman and John Isidor sought to promote clinical research by helping to safeguard the rights and welfare of clinical research subjects. As experienced lawyers and educators, John and Alan were well prepared to understand and implement the requirements laid out by the National Research Act of 1974, as well as applicable FDA regulations. As one of the first independent central IRBs, Schulman has maintained its position as an industry leader throughout its history.
Schulman’s team of dedicated professionals seeks to provide timely, quality services based on the foundation of respect for persons, beneficence and justice. Through continuous quality improvement and rigorous training on human subject protection, Schulman provides thorough, ethical, responsive and thoughtful review of research studies.
Since 1983 Schulman has provided the research community with IRB services of the highest caliber. As one of the leading accredited independent IRBs in North America, Schulman can provide IRB services for single and multi-site studies throughout the United States, Puerto Rico and Canada. By combining impeccable review standards, savvy industry insight, responsive customer service and innovative technological solutions, Schulman creates a review experience that goes beyond the expected. We’ve helped define the expectations. Now we’re redefining the experience.
Looking to select an IRB for your study? Learn why you should consider Schulman as your IRB.