We are a full-service Clinical Development Organization (CDO) with capabilities spanning from protocol development through to completion of full clinical study report.

The existing Evia team worked together for several years and most recently submitted an e-CTD to FDA. Our people are highly skilled, motivated, and have extensive experience, with a proven track record of clinical trial execution with excellence, meeting our commitments on time, and on budget.

Our collective experience and in depth knowledge spans multiple therapeutic areas, resulting in a wide network of clinical study sites and medical contacts.