In the highly regulated biotechnology sector, automating production processes is essential to ensure the quality and safety of pharmaceutical products. One of the major challenges faced by biotechnology researchers and production managers is to ensure product sterility while optimizing process efficiency. Our solution stands out as a state-of-the-art bioprocessing automation system, specifically designed to meet the stringent needs of the Big Pharma sector.
Our advanced bioprocessing automation technology is dedicated to the sterilizing filtration of vaccines and parenteral drugs before the filling stage. This system integrates critical features such as PUPSIT (Pre-Use, Post-Sterilization Integrity Testing), thereby guaranteeing filter sterility and integrity at every production cycle. With its compatibility with single-use systems, our solution easily interfaces with various integrity testing equipment and is adaptable to a wide range of sterilizing filters available on the market.
The system automates the transfer and final filtration of products, efficiently linking the finished product vessel to the filling machine. Its modular design allows seamless integration into different production environments while complying with the strict requirements of cGMP and GAMP5. Additionally, its compatibility with stainless steel piping technology and sterilizing filtration capabilities make this system a preferred solution for downstream bioprocessing.
This solution offers several competitive advantages for pharmaceutical industries:
| Elements | Processing range |
|---|---|
| Application |
|
| Filters |
|
| Flow Rate | Adjustable to filling equipment requirements |
| Dimensions | Customizable, with a minimum footprint of 850 x 1000 x 1975 mm |
| Frame |
|
| Electricity |
|
| Interface | 15″ or 17″ Touchscreen |
| Standard Integrity Testing Equipment |
|
| Integration |
|
| Data Monitoring |
|
| Certification |
|
