At QPS, a global full-service Contract Research Organization (CRO), clinical research services encompass comprehensive support for the development and approval of new therapies across all phases of clinical development. These services typically include study design, site selection, regulatory affairs, patient recruitment, clinical trial management, data collection and analysis, pharmacovigilance, and biostatistics, supported by robust laboratory services, such as preclinical studies (pharmacology and DMPK) and bioanalysis. With offices in USA, Europe, Asia, Australia, and India, and a site network of over 700 locations, QPS leverages local expertise and regulatory knowledge to streamline trial execution across multiple regions, ensuring compliance with international standards. By integrating cutting-edge technology and therapeutic expertise, QPS helps pharmaceutical, biotechnology, and medical device companies accelerate timelines, maintain excellence and bring safe, effective treatments to market more efficiently.

All services are conducted in accordance with ICH-GCP standards (International Conference on Harmonization-Good Clinical Practice) and local regulatory requirements to ensure consistent data integrity and patient safety.