Who Should Attend
• Formulation Scientists & Researchers: Professionals directly involved in the design, development, and optimization of sterile injectable formulations, including liposomes, nanosuspensions, microspheres, and other complex drug delivery systems or those planning to start work on complex injectables.
• Analytical Scientists: Experts responsible for developing and validating advanced analytical methods for the characterization of complex generics and demonstrating bioequivalence. This includes specialists in techniques like DLS, HPLC, and mass spectrometry.
• CMC & Regulatory Affairs Professionals: Individuals who prepare the Chemistry, Manufacturing, and Controls sections of regulatory filings and interact with agencies like the CDSCO, US FDA, and EMA for the approval and lifecycle management of generic injectables.
• Process Development & Manufacturing Engineers: Professionals who scale up lab-scale formulations to commercial manufacturing, focusing on sterile and aseptic processing, QbD implementation, and PAT.
other conference
06 - 07 Nov, 2025
Navigating Complexities in Pharmaceutical Analysis, Quality & Regulatory Compliance
