The Veeva Vault eTMF integration with Schulman's best-in-class WebPortal platform offers real-time IRB status information and approval documentation seamlessly and allows mutual clients to customize the interface to address unique needs. The integration offers users unparalleled transparency and efficiency and significantly reduces error rates and resource expenditure.
About Schulman IRB
Schulman 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, offering comprehensive solutions to maximize the protection of human subjects and improve overall quality standards for clinical studies and data integrity. 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 http://www.sairb.com or follow @SchulmanIRB on Twitter or on LinkedIn.
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SOURCE Schulman IRB