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PRESERVING THE INTEGRITY OF CLINICAL TRIALS

In the highly regulated and rapidly changing fields of pharmaceuticals, medical devices, genetics, and biotechnology, PSC Clinical is a leader in preserving the integrity of the process and the data for clinical trials and laboratory research. Our professional staff provides comprehensive clinical auditing, monitoring, data management, compliance, and other project management services to guard the quality of clinical research studies.

Clinical research sponsors can outsource any or all of the study management, quality control and compliance process to PSC Clinical with the assurance of unmatched quality at affordable prices. PSC Clinical professionals have worked on site in laboratories and academic medical centers across the U.S. and in major testing centers in China, India, Mexico, Brazil and other countries to ensure compliance with Good Clinical Practices and Good Laboratory Practices of the FDA and other regulatory boards. Our international monitors assure that both regulatory requirements and sponsor requirements are met across the globe – no matter where the trial is conducted.

We invite you to see why sponsors count on PSClinical to preserve the integrity of their work in developing lifesaving drugs, medical devices and treatments. Please contact us to discuss your specific requirements.

 

Services for Clinical Trials:

Clinical Trial Management
Clinical Monitoring
Medical Monitoring

Clinical Auditing

Data Management

Computerized System Validation

SOP Development

Good Clinical Practices Training


 

21CFR Part 11 Compliance
Quality Assurance
Process Development and Process Improvements
Best Practices Implementation

Report and Submission Development

Data and Trial Management Hosting

Protocol Development

Site Selection