Aseptic Manufacturing and Sterile Fill-Finish is a process where a drug product, container, and closure are sterilized. Next, the sterilized products are moved to a cleanroom to combine the products. Self-contained equipment is typically used during this process....
NNE has deep insight into aseptic and sterile fill and finish pharma processes. We can help you design and implement future-proof solutions for fill-finish operations, providing services within facility design, process engineering and automation and IT. Our know-how and expertise combines: ...
Fill-Finish Development Pii has over 25 years of experience managing the development of parenteral formulations forClinical Trialsand implementing scale up/Tech Transfer. Our four sterile fill-finish suites use single use technology in strict accordance with GMP requirements. ...
Over the last forty years technologies for the aseptic production of sterile products have advanced significantly. Where staffed clean rooms once provided most of the operational capacity, new production means have been gradually introduced. Isolator use began in the 1980s, to be followed...
blocks” (or, prefabricated single-use subassemblies) link together with sterile connection technologies. Regardless of size or configuration, all modular systems require reliable connectors to facilitate, protect, and manage fluid flow from the beginning of the process to final fill-and-finish. ...
RABS vs. Isolator Choosing the right isolation technology Learn more Fill/finish of liquid pharmaceuticals Syntegon expands local support for import projects in North America Learn more Aseptic and highly potent drugs Insights into state-of-the-art sterile fill/finish applications Learn more Inter...
• Fill finish inside a single-use disposable isolator • Handling of sterile potent powders • Isolator regulatory compliance • Sterilization: VHP vs Gamma Irradiation • Benefits of disposable isolator systems in sterile manufacturing