The QARP aids and advises pharmaceutical companies, CROs, and other healthcare organisations involved in drug development on GxP and Regulatory Affairs compliance with established worldwide standards. We assess overall compliance levels, focus on specific issues of concern and offer recommendations based on the broad experience of our auditors. We are creating an interactive platform to promote open discussions in the clinical research and quality management communities for all professionals and enhance professional skills through interactive workshops immersion into reality. We offer an exclusive program of interactive workshops, webinars, and online training in clinical research (advanced and basic Good Clinical Practice, ISO14155 Medical Devices, European Regulation on Clinical Trials and Medical Devices, Research Quality Management System, GCP audits methodology, etc.)