Partner with PRG to accelerate your clinical trials and drive breakthrough results

PRG handles Phase I-IV clinical trials to ensure high-quality data collection and patient care. They provide full-service trial management, including study acquisition, document handling, and provision of study-related equipment and supplies.

Dedicated recruitment teams are tasked with enhancing enrollment through various strategies, ensuring a robust trial participation rate. They also focus on patient retention by maintaining regular communication and support throughout the study.

Our team is skilled in utilizing advanced telemedicine platforms, remote monitoring tools, and electronic data collection methods that ensure reliable, real-time data capture while maintaining high patient safety and regulatory compliance standards. PRG’s experience in decentralized models allows us to create patient-centered trials that expand access, streamline study workflows, and deliver meaningful insights, making us a trusted partner for innovative, accessible clinical research solutions.

PRG ensures that all clinical trials comply with regulatory standards. They manage IRB submissions and communications, monitor safety, and handle adverse event reporting to maintain compliance with Good Clinical Practice (GCP) guidelines.

PRG offers state-of-the-art facilities for clinical trials, including private rooms, isolation rooms, and onsite pharmacy services. They ensure that all necessary equipment and supplies are available for the smooth running of trials.

PRG has extensive experience across various therapeutic areas, including allergy and immunology, dermatology, endocrinology, gastroenterology, infectious diseases, neurology, oncology, and more.

PRG provides comprehensive support for investigators, including training, study management, and administrative assistance, allowing them to focus on patient care and study conduct.