WHAT WE DO
We offer full Clinical Trial Management services including Clinical Project Management, Site Monitoring, Quality Assurance, Drug Safety, Payment Services, Biostatistics, Data Management, Regulatory Strategies, and Site Selection and Enrollment. PRC Clinical provides resources and support services to pharmaceutical and biotech companies conducting clinical trials. Our services span all phases of human trials, from Phase I studies in Healthy Subjects, through the Phase II, dose-finding and safety studies to larger Phase III and Post-Marketing studies. Learn more about our therapeutic experience.
Whether we are managing your entire study or providing regional monitoring, we promise unsurpassed service, rapid start-up, and the highest quality results in the industry. Our commitment to clients and sponsors means one-on-one attention and team driven efforts that go above and beyond “business hours” to produce results, keep investigator sites on track and sponsors informed. Our trial management staff offers expert resources to conduct the entire study or support focused aspects of each step along the development and regulatory pathway to approval.