For cell and gene therapy (CGT) and biopharmaceutical manufacturing processes, we supply everything from global brands to proven alternative brands, quickly.
Consumables, equipment and testing services for the entire process, from cell culture and cryopreservation to single-use, filtration, purification and QC, in one place. Our technical specialists work with you from product selection through process setup.
Corning Media · Buffer · FBS, BioLife Solutions, BioLamina
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Cobetter
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Cobetter
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Inscinstech, RJ Bio, Bestchrom, YMC
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SHENTEK, BRC Biotechnology
›Alongside global brand products, in areas where choices have been limited, such as filter membranes, resins and QC kits, we select and supply alternative manufacturers that have both the performance and the regulatory documentation.
We aim to supply the quantity you need when you need it, without the burden of long lead times and minimum order quantities.
Reasonably priced product lines that can be considered for the same process stage reduce the cost burden of process development and production.
From product selection through process setup and operation after adoption, our technical specialists provide consultation and technical support.
CryoStor® · HypoThermosol®, specified in more than 17 commercially approved cell therapies
View Brand ›ISO 13485:2016 QC kits · Method validation documents to USP, EP and ChP · Exclusive distribution in Korea
View Brand ›First Prize, 2023 China National Science and Technology Progress Award · Overseas subsidiaries in 4 countries
View Brand ›Founded in Kyoto in 1980 · Technical support from YMC Korea in Pangyo
View Brand ›The items above show only information cross-checked against the manufacturer's official materials and 2 or more independent sources.
A sterilizing-grade filter is defined not by its pore size rating but by a bacterial challenge test and process-specific validation. Based on the original regulatory documents, this guide covers what to check at the selection stage: the grade definition, material compatibility, integrity testing, sizing and supplier documentation.
Read ›This guide covers the main documents to request from suppliers when adopting a single-use system, what each document shows, and the regulations and standards behind them. Supplier data is input for the user's risk assessment, and responsibility for the assessment lies with the drug manufacturer.
Read ›Based on the original documents, this guide explains which documents recommend "10 ng/dose" and "approximately 200 bp" for residual host cell DNA and with what scope, and why there is no uniform numerical limit for host cell protein (HCP). It also covers what to check when choosing qPCR and ELISA test methods.
Read ›The SHENTEK full product catalog and materials for Inscinstech purification systems, Corning Media, YMC and GenCefe are provided as PDFs.
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Tell us your process stage and the product lines you need, and our technical specialists will respond quickly. TEL +82-2-6409-9338 · info@b2bio.co.kr
