CHI's Mastering Clinical Trial Monitoring


Changing FDA expectations, risk-based monitoring, and ever-growing demands for cost efficiency are fueling dramatic developments in the world of clinical research. Clinical trial monitors are on the front line of these changes, and must adapt to the world of centralized risk-based monitoring, quality systems-based approaches, and sophisticated technologies designed to improve outcomes. CHI will be addressing these issues at its sixth annual Mastering Clinical Trial Monitoring conference. Participants can expect to hear from thought-leaders to share their insights into addressing these challenges and exploiting these opportunities via presentations, case studies, and hands-on activities.

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Exhibitors

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