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Your Clinical Trial Deserves TLC From PRC

When You Need a Perfect Partner That Was Built to Match Your Needs

PRC Is the Right Clinical Research Organization for You

Since 2003, PRC Clinical has specialized in meeting the needs of pharmaceutical, biotech, and medical device sponsors through personalized clinical project management, feasibility, and site selection. Meet on-time enrollment goals via PRC’s site management, monitoring, and TMF trial document management services through Veeva Vault.

Our services span early phase trials, including Phase I studies, through Phase II to larger Phase III trials. Along with our technology tools to optimize clinical conduct, we offer a range of services, including clinical site management, project management, site selection, accelerated enrollment, and clinical data technology for streamlined metrics reporting through our network of strategic support partners.

PRC is dedicated to providing unparalleled support for trials with specialized patient populations, understanding that therapeutic areas including regenerative medicine, CNS, (Alzheimer’s, Parkinson’s, ALS), and ophthalmology require exceptional care. We partner with and nurture relationships with high-performing sites for optimized enrollment and data integrity. We work with some of the best industry research sites and experts, keeping the focus on your patients’ needs and the sensitivities of their conditions to ensure they remain enrolled and engaged throughout your program.

When You Need a Quality Relationship With Your CRO

Whether providing overall clinical trial management, North American support for global studies, remote, or site monitoring, PRC Clinical knows that highly specialized trials require hands-on care to deliver quality data. Driven by our nonstop use of cutting-edge technologies, we work closely with industry sponsors and sites to streamline your clinical trial operations, such as remote data review and online visit reports, surpassing the quality and personalized service offered by larger CROs. Our established Quality Management System (QMS) is built on the latest industry guidance and implemented to our highest quality standards, leveraging best practices and years of experience.

If You’re Looking for a Partner That Shares Your Values

PRC’s core values make us the right CRO partner for small-to-midsize biotech and medical device companies that value quality, data integrity, and personalized services. Our agile team of clinical trial experts, including project management staff, ensure you receive the consistent, hands-on support and resources needed to complete your study efficiently. Our team is committed to on-time delivery of your project, within scope, and ensuring we achieve your milestones, all while delivering unsurpassed service.

Does Your Trial Need TLC From PRC?

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