Compliance – Comprises of Comparative Dissolution Profiling (CDP), Photostability and Stability Study (SS), In-Use Stability Study (IUSS), Maintenance of Analytical Method Lifecycle, Quality Control (QC) of Starting Materials and Certificate of Analysis Generation for Investigational Medicinal Product (IMP).
To coordinate with supply chain personnel and plan, schedule and control production manpower, production cycle time and manufacturing equipment to ensure production schedules are met with measurable productive performance and efficiency.