PRC Clinical
PRC Clinical is a dedicated Contract Research Organization (CRO) with over 20 years of experience, specializing in supporting complex clinical trials across various therapeutic areas including regenerative medicine, CNS, ophthalmology, and more. They focus on delivering tailored trial management solutions, leveraging cutting-edge technology and deep therapeutic expertise to ensure studies stay on track and meet their goals. PRC Clinical emphasizes personalized service, experienced teams, and agility to navigate the challenges of clinical research, including regulatory compliance, site management, and patient recruitment. They serve pharmaceutical, biotech, and medical device sponsors, providing comprehensive support from study start-up to completion, with a strong track record of exceeding enrollment targets, managing global studies, and supporting innovative therapies.
Industries
Nr. of Employees
small (1-50)
PRC Clinical
South San Francisco, California, United States
Products
Full Service
A full-service model providing consistency across clinical operations, data management, safety oversight, and laboratory coordination from feasibility through database lock.
Full-Service CRO Support for Phase I Clinical Trial
PRC Clinical provided full-service CRO support to Xenome, an Australian biotech company, for a Phase I clinical trial involving 3 clinical sites for a neuropathic pain drug candidate.
Rescue & Mid-Study CRO Transition Services
PRC Clinical specializes in rescue and mid-study CRO transition engagements, supporting sponsors when trials are underperforming, disrupted, or at risk. Services include stabilizing operations, restoring site performance, recovering documentation and data integrity, and assuming operational ownership where needed.
PRC Clinical Rescue Project Service
A critical rescue project service executed by PRC Clinical involving the seamless transition of responsibilities from a U.S.-based CRO that ceased operations, integrating documentation into PRC Clinical's Veeva eTMF system to ensure compliance and timely outcomes.
Rare and Orphan Disease Trial Services
PRC Clinical offers specialized contract research organization services for rare and orphan disease clinical trials, including study management, study monitoring, eTMF and document management, and coordination and logistics support for Phase I through Phase III trials.
PRC Clinical Specialty CRO Services
Specialized contract research organization services with expertise in regenerative medicine, CNS, ophthalmology, pulmonary, COVID-19, rare and orphan diseases, and complex indications. Provides personalized clinical project management, feasibility assessments, site selection, and expert document management.
Full Service
A full-service model providing consistency across clinical operations, data management, safety oversight, and laboratory coordination from feasibility through database lock.
Full-Service CRO Support for Phase I Clinical Trial
PRC Clinical provided full-service CRO support to Xenome, an Australian biotech company, for a Phase I clinical trial involving 3 clinical sites for a neuropathic pain drug candidate.
Rescue & Mid-Study CRO Transition Services
PRC Clinical specializes in rescue and mid-study CRO transition engagements, supporting sponsors when trials are underperforming, disrupted, or at risk. Services include stabilizing operations, restoring site performance, recovering documentation and data integrity, and assuming operational ownership where needed.
PRC Clinical Rescue Project Service
A critical rescue project service executed by PRC Clinical involving the seamless transition of responsibilities from a U.S.-based CRO that ceased operations, integrating documentation into PRC Clinical's Veeva eTMF system to ensure compliance and timely outcomes.
Rare and Orphan Disease Trial Services
PRC Clinical offers specialized contract research organization services for rare and orphan disease clinical trials, including study management, study monitoring, eTMF and document management, and coordination and logistics support for Phase I through Phase III trials.
PRC Clinical Specialty CRO Services
Specialized contract research organization services with expertise in regenerative medicine, CNS, ophthalmology, pulmonary, COVID-19, rare and orphan diseases, and complex indications. Provides personalized clinical project management, feasibility assessments, site selection, and expert document management.
Services
Operational oversight and tailored program management for clinical studies, from protocol planning to study close-out.
Electronic TMF administration, document migration, QC, and inspection readiness services for study documentation.
Provision of experienced CRAs for monitoring visits, e-visit reporting, and monitoring program execution.
Coordination of vendors, central labs, investigational product packaging and storage, and sample shipment logistics for multi-site and global studies.
Rapid audit, data recovery, and operational takeover services to transition studies mid-course and restore study momentum.
Operational oversight and tailored program management for clinical studies, from protocol planning to study close-out.
Electronic TMF administration, document migration, QC, and inspection readiness services for study documentation.
Provision of experienced CRAs for monitoring visits, e-visit reporting, and monitoring program execution.
Coordination of vendors, central labs, investigational product packaging and storage, and sample shipment logistics for multi-site and global studies.
Rapid audit, data recovery, and operational takeover services to transition studies mid-course and restore study momentum.
Expertise Areas
- Clinical trial management
- Site management and monitoring
- CRO transition and rescue operations
- Regulatory support for US and international trials
Key Technologies
- Electronic trial master file (eTMF) platforms
- Cloud-based Clinical Trial Management Systems (CTMS)
- Validated electronic signature systems
- Remote/centralized monitoring tools
News & Updates
Celebrating 20 Years of PRC Clinical
Celebrating 20 Years of PRC Clinical
An article discussing the challenges and advancements in stem cell research.
Insights into improving research methodologies in psychedelics studies.
Strategies for effective patient recruitment in clinical trials.
Successfully exceeded enrollment expectations for a U.S. chronic kidney disease study, enrolling more patients than projected.
Celebrating 20 Years of PRC Clinical
Celebrating 20 Years of PRC Clinical
An article discussing the challenges and advancements in stem cell research.
Insights into improving research methodologies in psychedelics studies.
Strategies for effective patient recruitment in clinical trials.
Successfully exceeded enrollment expectations for a U.S. chronic kidney disease study, enrolling more patients than projected.