At DPQSS, we believe that Data, Process, and Quality (DPQ) are the fundamental pillars that drive organizational success. Our commitment to these pillars ensures that we support your organization in reaching the same level of excellence.
At DPQSS, our mission is to foster success by upholding the values of Good Data, Robust Processes, and Strong Quality Systems for achieving operational excellence:
This mission combined with our values are the foundation of our approach, enabling us to provide superior solutions and services to our client
DPQSS provides global consulting services in clinical research, non-clinical studies, medical services and in vitro studies. We offer services for Monitoring, auditing, Quality Management, Project Management, Pharmacovigilance, training and software validation. Committed to the highest global quality standards, our experienced team provides customized solutions for data, processes, and quality systems to achieve compliance.
RQAP GCP
Global clinical research professional with over 16 years of diverse experience in clinical operations, quality assurance, data management, and project management within global pharmaceutical companies, CROs, and BPO companies for clinical research and medical affairs. Successfully managed multiple regulatory inspections and conducted audits in India and abroad. The experience includes phase 1-IV clinical trials, BA/BE studies, patient PK studies, RWE/PMS studies. This unique background of working with both sponsors and service providers in multiple roles combined with exposure to different various study set-ups allows to deliver tailored services by understanding perspectives from both ends.
Co-founder, Director Operations
Global Clinical Research professional with over 18 years of diverse experience in global and domestic Sponsor and CRO companies. Proficient in managing multiple phase I-IV trials, achieving milestones ahead of schedule through expert oversight and project management. Involved in Strategic discussions and technically sound protocol development which has resulted into the successful clinical trials for global Sponsor organisations. Skilled in various therapeutic areas for global regulatory submissions and has a successful track record in clearing site audits and inspections.