Media Fill test procedure | Aseptic Process Simulation APS | How to GMP tutorial | pharma industry

Related videos to boost your knowledge:

   • What is Alcoa? Data Integrity in pharmaceu...  

   • Deviations in Pharmaceutical Industry 💊 De...  

   • CAPA in Pharmaceutical Industry [2026 Guide]  

   • Project Management in pharmaceutical indus...  

   • 10 Golden rules of GMP [2026] | Free GMP T...  

   • How to qualify HPLC: Qualification Explain...  

   • Change Control in pharmaceutical Industry ...  

   • Batch Record Review [FULL GMP Training in ...  


In this comprehensive tutorial, we will guide you through the Media Fill test procedure, a crucial step in Aseptic Process Simulation (APS) for the pharma industry. The Media Fill test is an essential validation process for sterile drug manufacturing, ensuring Good Manufacturing Practice (GMP) compliance. We will cover the importance of contamination control, environmental monitoring, and microbiology in aseptic processing. You will learn how to validate an aseptic process, including aseptic fill finish, RABS, and Restricted Access Barrier Systems. Our expert, Dhaval Surti, will walk you through the process, providing valuable insights into pharmaceutical quality, quality management, and sterilization. This tutorial is perfect for those looking to understand the principles of aseptic processing, including cleanroom operations, validation, and GMP compliance for sterile drugs. By the end of this video, you will have a thorough understanding of the Media Fill test procedure and its application in the pharmaceutical industry.