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Schulman IRB to Exhibit at Arena Outsourcing in Clinical Trials Southeast

Schulman IRB will be exhibiting at the 6th Annual Arena Outsourcing in Clinical Trials Southeast 2017 from March 21-22 at the Embassy Suites in Cary, North Carolina.

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Schulman IRB Reaches Over 1,000 Contractual Relationships with Research Institutions

Schulman IRB holds over 1,000 contractual relationships with research institutions, including agreements with individual institutions and broader agreements with healthcare systems and reliance networks.

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ACRP Features Schulman IRB Biosafety Officer

Daniel Eisenman, PhD, RBP, SM(NRCM), CBSP, Biosafety Officer at Schulman IRB, discusses the emphasis on biosafety in clinical trials in an ACRP article.

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Exclusive Free Symposium on Federal Initiatives Toward Single IRB Review

Schulman IRB Connections Presents: Emerging Issues in Research – Federal Initiatives Toward Single IRB Review Join industry colleagues February 15 for an interactive presentation and discussion of emerging issues in research. *This event has concluded. Thanks to everyone who joined the conversation in Boston!* Recent federal initiatives make it clear that the US government favors […]

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Applied Clinical Trials Features Article on 21st Century Cures Act

Applied Clinical Trials recently featured an article written by Michele Russell-Einhorn that outlines the provisions of the 21st Century Cures Act.

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Schulman IRB Adds Biosafety Officer to Team

Schulman IRB announces that Daniel Eisenman, Ph.D., RBP, SM(NRCM), CBSP, has joined the organization as Biosafety Officer.

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Schulman IRB Becomes Veeva Technology Partner

Schulman IRB, the industry-leading central IRB in customer service and technology, announces its integration with Veeva Systems.

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Final Revisions to Common Rule Now Available

HHS and 15 other federal agencies have issued the final rule to update US regulations that safeguard research participants.

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