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Researchers have witnessed a vast change in the clinical research environment regarding the protection of research participants. The desire to maximize both efficiency and participant protection ranks high on the priority list of many clinical researchers. As such, the issue of “Streamlining the Clinical Research Enterprise” was taken up in a workshop by the Clinical Research Roundtable (CRR) to discuss whether the perceived regulatory burden is due to regulations or other components of the clinical research enterprise.
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Keck Center500 Fifth St. NWWashington, DC 20001