When You Need Special Handling for Your Specialized Research
Clinical trial conduct is a complex process requiring an experienced partner with the agility and tenacity to creatively push through critical study challenges. PRC Clinical knows that highly specialized early-phase trials require a high-touch approach to ensure high-quality results.
With our specialized expertise in regenerative medicine, ophthalmology, and CNS, PRC works hand-in-hand with sponsors to determine an effective approach for your patient population. Our team of experts complements your team, providing an extra level of oversight to support on-time delivery of your project — within budget.
We work as your liaison, closely monitoring sites and collaborating with you to coordinate all activities, including training, patient recruitment, and reporting. Following gold-standard processes, our experienced project managers and CRAs ensure investigators are appropriately selected and trained to complete your study efficiently, while also nurturing relationships with all sites to guarantee quality, on-time deliverables.
To meet milestones, we strive to provide seamless data flow and transparent communication throughout the study life cycle. Our entire study team goes the extra mile to account for even the smallest aspect of your project, so you can rest assured that your trial is being handled with the utmost care.
If You Need a High-Touch Approach
The PRC Approach Is Right for You
With broad therapeutic experience and focus on regenerative medicine, we’ve purpose-built our approach to match you at every step with the technology, processes, and expertise needed for high-quality, efficient execution. Since every project is unique, we never force yours into a templated set of processes or systems that don’t factor in the needs of your patient population. Our expert team was created with yours in mind, with the agility to scale to match your needs and the drive to go the extra mile.
When You Need Vast Biotech Experience
PRC Clinical Has the Right Expertise
Over 15 years of experience moving innovative biotech and drug development projects forward with the clinical and operational guidance needed to successfully advance.
Ability to rapidly scale our approach to match the needs of even the most complex projects.
Expertise within regenerative medicine studies, therapeutic expertise with neurology trials for Parkinson’s, Alzheimer’s, and ALS, as well as ophthalmology and pulmonary trials.
We understand the need to be prepared. Relying on our existing business continuity plans, PRC is able to immediately respond to the needs of our clients to maintain trial momentum. When the COVID-19 pandemic began, we were capable of quickly modifying long-term plans and best practices for permanent use. Our flexible team is dedicated to working closely with you to create personalized strategies and customized solutions to navigate current challenges, including remote monitoring, decentralized trial support for COVID trials and more.
If Your Trial Needs Extra Resources
PRC Has the Right Partnerships
Cytel has over 30 years of industry and academic research experience. Cytel’s services range from providing data management, biostatistics, and DMC support to medical writing, statistical report writing, statistical genetics and genomics services, and custom web-based data collection tools. Cytel’s experience includes projects ranging from small-scale data management to complex multicenter studies with hundreds of sites and thousands of patients.
Cenetron is an industry leading central laboratory, supporting global studies in Phase I through Phase IV clinical trials. Cenetron offers complete central laboratory services, including sample storage and kit manufacturing facilities, and specializes in custom assay development and companion diagnostic tests to provide the latest tools for screening, randomizing, and monitoring patients.
With over 15 years of experience, SDC delivers leading-edge statistical analysis and data management services with biostatistics, clinical data management/EDC, and interactive response technology (IRT) expertise. SDC offers engaged experts alongside top-tier clinical trial services.
Veeva Vault is a true cloud enterprise content management platform and suite of applications specifically built for life sciences. Veeva Vault is the only content management platform with the unique capability to manage both content and data. Because all Vault applications are built on the same core platform, companies gain additional efficiency and compliance through the streamlined flow of documents across regions and departments. Content stays accessible, current, and in context across the entire development and commercial life cycle.
The pioneer of independent ethical review, WCG continues to drive ingenuity in the clinical research space. WCG’s solutions have grown to include a suite of complementary services to support contract management and pharmacovigilance among other ancillary trial services.
PRC Clinical is proud to be an active sponsor and supporter of ACRP. The association supports clinical research professionals through membership, training and development, and certification. Founded in 1976, ACRP is a Washington, D.C.-based nonprofit organization with more than 13,000 members who work in clinical research in more than 70 countries. ACRP’s vision is that clinical research is performed ethically, responsibly, and professionally everywhere in the world. ACRP’s mission is to promote excellence in clinical research. In 2016, PRC Clinical received the Annual Sponsor Award from the ACRP Northern California Chapter.