Pharmaceutical and Biotechnology Filtration & Processing
Our solutions are designed to perform reliably in controlled, hygienic, and highly regulated manufacturing settings where product quality and process performance are paramount.
From raw water and utility systems to process fluids and support services, effective filtration is essential throughout pharmaceutical and biotechnology facilities. New World Filtration designs and supplies filtration and separation systems that manage particulates, microorganisms, liquids, and process contaminants that can compromise production stability and equipment performance.
All solutions are engineered for cleanability, reliability, and compatibility with hygienic process environments.
- Adsorptive depth filtration
- Endotoxin and bioburden reduction
- Sterilizing grade filtration (liquid and gas)
- Solvent and bulk chemical filtration
- Stability chambers
- High purity tubing, hose and single use systems
- Improved process stability and batch-to-batch consistency
- Protection of high-value manufacturing and support equipment
- Reduced risk of contamination-related disruptions
- Enhanced reliability of utility and support systems
- Lower maintenance frequency and lifecycle costs
- Improved uptime in continuous and batch operations
Operational & Performance Benefits
Delivering measurable value across pharmaceutical and biotechnology manufacturing facilities:
Active ingredients used in the pharmaceutical industry contain impurities that result from chemical reactions. These reactions produce colored by-products. These are removed using activated carbon. This is necessary to maintain the purity of the drug.
Drugs may also contain dissolved solids that need to be reduced in order to comply with product quality standards and ensure safety as well.
Drugs may also contain dissolved solids that need to be reduced in order to comply with product quality standards and ensure safety as well.
Controlling bioburden is important to improve processes in the pharmaceutical industry. Endotoxin and bioburden reduction leads to clarification of process streams.
Sterilizing grade filtration requires robust filters that are designed by regulatory authorities in accordance with the established standards ( like retaining specific microbes etc. ).
The process of removal and recovery of solids is used in the pharmaceutical industry at various stages of drug production.
Solvents and chemicals are used in bulk for production of active ingredients in pharmaceutical industries. These chemicals contain particulates which are removed by filtration. The process of chemical and solvent filtration ensures the quality of the product.
The stability chambers are made as per cGMP and GLP requirements. Walk-in stability chambers are used for stability studies (checking stability of a drug under different environmental conditions).
These products reduce the risk of contamination and increase efficiency. Moreover, they also reduce the risk of leakages.