Schulman Associates IRB, Inc.

Schulman Associates IRB has been a leader in the protection of human research participants in the U.S., Puerto Rico and Canada since 1983. Schulman offers thorough, timely IRB review services – including dedicated review capabilities for all phases of research across all therapeutic areas – to clinical trial sponsors, CROs, investigators and institutions. Schulman also provides global consulting services through its joint venture partner Provision Research Compliance Services, offering comprehensive solutions to improve overall quality standards for clinical studies and data integrity, and to maximize the protection of human subjects. Fully accredited by the Association for the Accreditation of Human Research Protection Programs (AAHRPP), Schulman has an unparalleled clean audit history with the Food and Drug Administration (FDA).

For more information, please visit or follow @SchulmanIRB on Twitter or on LinkedIn.

Contact Information

Main Offices -

P. (513) 794-5775
4445 Lake Forest Drive
Suite 300
Cincinnati, OH 45242
Media Contact Name: Stephanie Pyle

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Consulting, Technology

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Cincinnati, Raleigh

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