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Your Clinical Trial Deserves TLC From PRC

Expert Clinical Trial Oversight

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The Big Picture

PRC Clinical was purpose-built to give your early phase pivotal study the superior attention it deserves. With services and expertise spanning Phase I to Phase III, PRC provides the clinical study oversight and support needed to deliver safe and efficient clinical research, ensuring your trial is successful.

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Study Oversight

PRC Clinical is a unique CRO that stands out due to its focus on clinical study oversight and project management. Our team comprises expert project managers and tenured regional CRAs who work together to ensure accountability and timely delivery of projects. We cater to small-midsize biotech, pharma, device and diagnostic companies, providing personalized support, solutions and resources to meet their specific needs.

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Enrollment

Our large network of clinical trial sites can help you overcome the challenge of selecting the right site and enrolling patients for your trial. With our optimized selection, management and monitoring, we ensure study activation and ongoing reliability. Let us help you speed up your clinical trial process.

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Site Management

Our team of experienced project managers and CRAs are dedicated to superior clinical site management, ensuring that your study is conducted in compliance with GCP and ICH guidelines, as well as regulatory requirements. We carefully select and train investigators to ensure high-quality results, providing you with the support you need to achieve success.

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Vendor Management

Our team at PRC is dedicated to your study’s success, providing comprehensive clinical study oversight to ensure that all study deliverables are of the highest quality and provided on time. To achieve this, we will collaborate with other study vendors, providing oversight and management to ensure that all project goals are met. We are committed to delivering exceptional results and exceeding expectations.

Mid-Study Transitions

At PRC, we take pride in our ability to rescue studies that are in danger of failing due to the original CRO chosen. Our extensive experience and expertise has enabled us to successfully help numerous sponsors turn their trials around by transitioning the study mid-stream. We understand the importance of ensuring the success of your study, and we are committed to providing professional guidance and support throughout the process. With PRC on your side, you can have confidence in the outcome of your study and data.

Does Your Trial Need TLC From PRC?

Let’s Talk