Pharma Knowledge

Pre-operational sanitation is the most underestimated yet decisive phase in the lifecycle of any pharmaceutical system. It represents the moment when a newly installed utility or manufacturing system transitions from being an engineered structure to becoming a GMP-relevant process element. Unlike routine cleaning, pre-operational sanitation is not about maintenance—it is about origin control. A system … Read more

The “Immune System” of Pharmaceutical Manufacturing** Imagine pharmaceutical manufacturing as a living organism—complex, sensitive, and continuously challenged by threats: deviations, failures, drifts, outliers, and non-conformities. Now imagine CAPA as the immune system of that organism—detecting harmful events, attacking the cause, and building future immunity so the same threat can never harm the system again. In … Read more

(Commonly Known as Smoke Study in Cleanroom Areas) Airflow Visualization Studies (AVS) are qualitative yet powerful tools used in cleanroom environments to make invisible air movement visible. Instead of relying only on numerical airflow data, this study uses generated smoke or fog to visually demonstrate how air behaves around critical processing zones, equipment, operators, and … Read more

Sterile Active Pharmaceutical Ingredient (API) manufacturing is a world where invisible microbes are the enemy, aseptic discipline is the shield, and process integrity is the battlefield. The Media Fill Test (MFT)—often called Aseptic Process Simulation (APS)—is the ultimate “dress rehearsal,” designed to prove that a sterile manufacturing line can function flawlessly before a real API … Read more