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Email ：PharmaSources@imsinoexpo.com
Whatsapp ：+86-13621645194
Main Sales Markets: North America,Central/South America,Western Europe,Eastern Europe,Australasia,Eastern Europe,Australasia,Asia,Middle East,Africa
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Homogenate tank & Process tank tube system
Homogenate tank is suitable for homogenate storage and mixing when large scale chromatographic column is filled.
Portable design for easy use and maintenance.
Provide low shear force uniform stirring, circulation device to ensure that the filler evenly mixed.
Tank material: 316L stainless steel.
Upstream and downstream process tank system
Strategic partners cover the entire biopharmaceutical process from cell culture/fermentation - harvest - isolation and purification - formulation.
For example: culture medium preparation system, feeding system, buffer preparation system, buffer storage system, chromatographic sampling system, ultrafiltration system, nanofiltration system, preparation liquid dispensing system, and supporting CIP system and so on. Pharmaceutical engineering has been involved in recombinant anticancer drugs, monoclonal antibodies, insulin, fat milk, etc.
Automatic dispensing
Multiple groups of instruments online monitoring, parameter feedback adjustment, accurate proportional control, accuracy ±2% (flow rate, conductance).
Improve efficiency, reduce labor, reduce time.
Reduce the area of liquid storage tank, use now, convenient and fast.
Liquid dispensing, chromatography is carried out at the same time, and the whole process of liquid dispensing is recorded electronically.
Dilution times from several times to dozens of times, can be customized according to customer process design.
Ultrafiltration/nano filtration
Biocompatible high flow rate pumps are preferred to fully meet the experimental and cleaning needs of pharmaceutical companies.
Using standard industry touch screen computer control, the software meets the requirements of FDA 21 CFR Part11.
Online detectors such as conductivity, PH value, temperature and multi-wavelength ultraviolet absorption can be configured in the system to record the running curve according to the process requirements.
Automatic CIP program can be set up.
Full process monitoring records, in compliance with FDA and CGMP regulations.
Audited Supplier
Pharma Sources Insight June 2024: Globalization on the Go
