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Changing the Paradigm
of Clinical Research

CRA Manages Study Regulatory

In addition to clinical oversight, CRA has facilitated research at sub-sites by establishing centralized regulatory management and contractual services.

This centralization expedites the research process, so that sub-sites need not worry about the ‘nitty-gritty’ of conducting clinical trials, such as submission to an IRB, negotiation of the contract, sending out regulatory documents for study start-up, maintaining a study file, and other clinical requirements.

Our capable research team handles all these aspects. Without having to concern themselves with these, sometimes tedious, facets of clinical research, physicians and clinical personnel can focus solely on patient care and still have the opportunity to enroll their patients on clinical trials.