Place of Origin : Huaian,China
Biopharm purification equipment independently developed by Hanbon includes Chromatography columns, Chromatography system, In-line buffer dilution system, Filtration system, Single-use system, etc. The device software meets the requirements of GLP/GMP regulations and FDA 21CFR part 11 requirements and has a complete IQ/OQ/PQ verification file system that can provide document support for user GMP/FDA certification.
Hanbon's Chromatography Systems, Filtration Systems, In-line Dosing Systems, And Other Products Are Inextricably Linked To The Separation And Purification Of Antibody Drugs And Are Essential Tools For The Preparation Of High-quality Antibody Drugs, Both In The Process Development And Production Stages.
Application Of Chromatography And Filtration Techniques In Antibody Purification
Vaccines Are An Effective Means Of Preventing Infectious Diseases. In The Process Of Vaccine Preparation, Viruses Or Bacteria Need To Be Produced First By Cell Culture, Etc., And Then Inactivated And Lysed To Obtain The Vaccine Stock Solution. Next, The Vaccine Stock Solution Needs To Be Isolated And Purified To Obtain A High-purity Vaccine Product. In This biopharma Purification Process, Hanbon's Chromatography System And Ultrafiltration System Can Be Used To Separate And Purify The Target Proteins In The Vaccine Stock Solution To Obtain A High-purity Vaccine Product. Specifically, Affinity Chromatography, Ion Exchange Chromatography, And Gel Chromatography Can Be Used To Remove Impurities From The Vaccine Raw Material Solution To Obtain High Purity Vaccine Products.
For More Information about biopharma Downstream Processing, Please Feel Free To Contact Us!
