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Delays in clinical studies hurt

by Gretchen Bowker | Mar 17, 2011

How do we get study timelines back on track?

Check it out… http://www.rxtrialsinc.com/our-blog/

Single IRB – A Guide to the Common Rule sIRB Mandate

The sIRB requirement is active. Is your study affected?

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Clinical Research Accelerated

You need high quality, timely board reviews so that you can get your study in the clinic.

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Pearl IRB is an independent institutional review board, fully accredited by the Association for the Accreditation of Human Research Protection Program Inc. (AAHRPP).  Pearl IRB manages the local and central IRB needs for large and small institutions, principal investigators, CROs, and sponsors. Our vision is to improve the clinical research process which will lead to delivering therapeutics and diagnostics to patients sooner. Whether the research is a small single site project or a complex multi-center study, we can help.

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