Your Premier Contract Research Organization

At Pacific Clinical Research, a respected Contract Research Organization, we manage all aspects of your trials. Experience seamless execution of your clinical trials. Our expert team manages all aspects of your trials, from planning and site selection to data collection and final reporting, ensuring efficiency and integrity throughout the process.

Maintaining oversight of your clinical trials is crucial. Our clinical monitoring services are designed to ensure compliance with protocols, perform site inspections, and validate the integrity of collected data, assuring the success and reliability of your trials.

Clear and concise communication is essential in clinical research. Our team of skilled medical writers craft detailed protocols, comprehensive reports, and regulatory documents that are scientifically accurate, clear, and compliant with guidelines.

Patient safety is our utmost priority. We provide robust pharmacovigilance and drug safety services, including adverse event tracking, safety reporting, and risk management, to ensure the highest standards of patient safety and regulatory compliance.

Effective documentation is the backbone of successful clinical trials. Our Trial Master File (TMF) management services ensure that all necessary trial documentation is accurately maintained, readily available, and audit-ready, supporting a smooth and compliant trial process.

Maintain the highest standards in your clinical trials. Our quality assurance team conducts thorough audits and inspections, monitors compliance with Good Clinical Practice (GCP), and ensures that all aspects of your trials meet stringent quality standards.