Capsule Filters

In the precision-driven world of biopharmaceuticals, every milligram of your target molecule is vital. We are dedicated to providing superior separation and purification solutions designed to ensure purity, maximize recovery, and enhance operational efficiency—accelerating your journey from R&D through to commercial manufacturing.

• Inherent Hydrophobicity
• High Retention Rate
• High Flux
• Low Differential Pressure
• Reliable bacterial and particulate retention

• Unique double-layer design
• Reliable bacterial and particulate retention
• Broad chemical compatibility, pH 1-14
• Extremely low extractables

• Reliable bacterial and particulate retention
• Broad chemical compatibility, pH 1-14
• Extremely low extractables
• Low protein binding

Reliable bacteria and particulate retention, broad chemical compatibility, high flow rates, and high throughput.

Challenge IM offers a comprehensive portfolio of capsule filters, including Clarification, Pre-filtration & Bioburden Reduction, Sterilizing-grade, Mycoplasma Removal, and Gas Filtration series. With a wide retention range from 0.1μm to 30μm, our solutions support the entire bioprocess workflow—from cell culture clarification to final product sterilization.

Scientifically graded multi-layer structure using Polypropylene (PP) membranes of different pore sizes, featuring high retention efficiency, high throughput, and high dirt holding capacity.

The Challenge IM Capsule Filters cover five key series: clarification, pre-filtration & sterilizing-grade, sterile, mycoplasma removal, and gas filtration, with particle retention ranging from 0.1 to 30 μm, meeting the full process requirements from cell culture clarification to final product sterilization. The filters support high-temperature steam sterilization and gamma irradiation, and are compatible with a wide range of commonly used biopharmaceutical solvents. All molded parts and sealing components are free of colorants and comply with Class VI and ISO 10993 biocompatibility standards, minimizing leachables and extractables and ensuring hygienic processing. Each product undergoes dual integrity testing during production, with two independent test methods required for release, ensuring 100% factory pass rate. The filters comply with ISO 9001 quality management and GMP standards, and have passed USP <85> endotoxin, USP <87>/<88> biocompatibility, and USP <665> extractables tests, with no animal-derived TSE/BSE risk. All products are validated by multiple internationally recognized agencies such as SGS and NF, providing fully verified and reliable filtration solutions for the entire biopharmaceutical process.

The single-use, fully automated tangential flow filtration (TFF) system is built with GMP-compliant fluid contact materials and delivers efficient, flexible filtration solutions to meet production needs from clinical development to commercial manufacturing. It offers intuitive operation and seamless scalability across different process scales, helping users significantly reduce production time and costs. The system is widely applied in the manufacturing of monoclonal antibodies, ADCs, gene therapies, viral products, mRNA vaccines, and plasmid DNA, supporting processes such as concentration, purification, and continuous buffer exchange.

The Challenge IM Capsule Filters cover five key series: clarification, pre-filtration & sterilizing-grade, sterile, mycoplasma removal, and gas filtration, with particle retention ranging from 0.1 to 30 μm, meeting the full process requirements from cell culture clarification to final product sterilization. The filters support high-temperature steam sterilization and gamma irradiation, and are compatible with a wide range of commonly used biopharmaceutical solvents. All molded parts and sealing components are free of colorants and comply with Class VI and ISO 10993 biocompatibility standards, minimizing leachables and extractables and ensuring hygienic processing. Each product undergoes dual integrity testing during production, with two independent test methods required for release, ensuring 100% factory pass rate. The filters comply with ISO 9001 quality management and GMP standards, and have passed USP <85> endotoxin, USP <87>/<88> biocompatibility, and USP <665> extractables tests, with no animal-derived TSE/BSE risk. All products are validated by multiple internationally recognized agencies such as SGS and NF, providing fully verified and reliable filtration solutions for the entire biopharmaceutical process.

The Challenge IM Capsule Filters cover five key series: clarification, pre-filtration & sterilizing-grade, sterile, mycoplasma removal, and gas filtration, with particle retention ranging from 0.1 to 30 μm, meeting the full process requirements from cell culture clarification to final product sterilization. The filters support high-temperature steam sterilization and gamma irradiation, and are compatible with a wide range of commonly used biopharmaceutical solvents. All molded parts and sealing components are free of colorants and comply with Class VI and ISO 10993 biocompatibility standards, minimizing leachables and extractables and ensuring hygienic processing. Each product undergoes dual integrity testing during production, with two independent test methods required for release, ensuring 100% factory pass rate. The filters comply with ISO 9001 quality management and GMP standards, and have passed USP <85> endotoxin, USP <87>/<88> biocompatibility, and USP <665> extractables tests, with no animal-derived TSE/BSE risk. All products are validated by multiple internationally recognized agencies such as SGS and NF, providing fully verified and reliable filtration solutions for the entire biopharmaceutical process.