Products

Biotechnology involves the use of microorganisms and biological processes; the most common examples are fermentation, cell culture, filtration and purification. The application of these techniques extends to the production of antibiotics, hormones, enzymes, vaccines, recombinant proteins, monoclonal antibodies etc. in biotechnology and biopharmaceutical industry. 

Fermenters & Bioreactors are designed to contain an internal environment for the optimal metabolization and efficient propagation of microorganisms or cell culture. These are also designed in a way to avoid contamination, beginning as aseptic spaces. These are either designed for batch culture or continuous culture. Fermenters are majorly used to propagate micro organisms where as Bioreactors are used to propagate cell culture. The Design requirements vary for both these equipments which need a good understanding of customer process and bioprocess engineering. We offer fully automated standard Fermenters & Bioreactors along with customized one from the range of 10 – 20000 L in Stainless Steel (with or without CIP) and Single Use. Our design ensures long-term sterility and maintenance of exact process parameters to ensure the maximum yield. We make sure that we strictly follow ASME BPE & US FDA guidelines to meet all the safety and quality criteria.

Filtration & Purification Skid Systems are based either on cartridge filtration technology or Crossflow filtration/tangential flow filtration technology.We offer fully automated/manual standard cartridge filtration along with customized one to ensure the removal of specific particles by microfiltration. The skids are designed to have single or multiple filtration/purification stages in Stainless Steel (with or without SIP/CIP) and Single Use.
Crossflow filtration or tangential flow filtration is a type of filtration which is different from dead-end filtration. In Crossflow filtration or tangential flow filtration the feed flow travels tangentially across the surface of the filter, which causes the filter cake or filter gel get washed away along with the filtration process. This mode of filtration can be operated either in batch or continuous mode. The main driving force of cross-flow filtration process is transmembrane pressure which is the pressure difference between two sides of the filter membrane. This process could be used for the isolation/separation of cells in fermentation or cell culture process, concentration of bio-molecules or diafiltration to eliminate the molecules which are not the subject of interest. We offer fully automated/manual standard Crossflow filtration or tangential flow filtration skids along with customized one from the range of 0.1 to 56 sq.meter in Stainless Steel (with or without SIP/CIP) and Single Use. Our design ensures long-term sterility and maintenance of exact process parameters to ensure the maximum yield. We make sure that we strictly follow ASME BPE & US FDA guidelines to meet all the safety and quality criteria.

We offer fully automated/manual Process vessels for production of Sterile products, Media & Buffer preparation etc. from the range of 10 – 20000 L in Stainless Steel (with or without SIP/CIP) and Single Use.Our design ensures long-term sterility and maintenance of exact process parameters to ensure the maximum yield.

We make sure that we strictly follow ASME BPE & US FDA guidelines to meet all the safety and quality criteria The Process Vessels can either be mobile or stationary.

Cleaning-In-Place and Sterilizing-In-Place systems are an integral part of biotechnology and bio pharmaceutical industry.We offer high-performance automated/manual CIP & SIP skids that are customized to the client's specific requirements. The CIP & SIP Skids can either be mobile or stationary.which controls and monitor allThe CIP Skids vary from small mobile units without any vessel which can be hooked up to any bioprocess vessels/systems to four tank central CIP units which could centrally cater the CIP needs of a whole plant as per the GMP guidelines. The SIP Skids can be hooked up to any bioprocess vessels/systems to do the sterilization in place of the same, which controls and monitor all the SIP parameters as per the GMP guidelines. Our design ensures long-term sterility and maintenance of exact process parameters. We make sure that we strictly follow ASME BPE & US FDA guidelines to meet all the safety and quality criteria.