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Mab-Venture Biopharma

Shanghai, CN

Mab-Venture was established in early 2014 in Shanghai’s Zhangjiang Hi-Tech Park. It is an integrated biotechnology CRO/CDMO dedicated to supporting global biopharma from discovery to GMP manufacturing. Mab-Venture is also committed to developing a biopharmaceutical research and development platform. In May 2015, Mab-Venture built a new 20000 sq.ft. R&D and pilot production base in Shanghai’s Zhangjiang International Medical Park. In March 2017, Mab-Venture built an additional 35000 sq.ft. GMP manufacturing facility. The two facilities provide an end-to-end solution from research to four pilot production lines to support biologics development and manufacture in the pre-clinical and early clinical stages. R & D equipment investment thus far has been >$20 million dollars. The Mab-Venture team is just over 100 people and is expanding rapidly, with headcount expected to be over 150 by the end of 2017.

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Mab-Venture was established in early 2014 in Shanghai’s Zhangjiang Hi-Tech Park. It is an integrated biotechnology CRO/CDMO dedicated to supporting global biopharma from discovery to GMP manufacturing. Mab-Venture is also committed to developing a biopharmaceutical research and development platform. In May 2015, Mab-Venture built a new 20000 sq.ft. R&D and pilot production base in Shanghai’s Zhangjiang International Medical Park. In March 2017, Mab-Venture built an additional 35000 sq.ft. GMP manufacturing facility. The two facilities provide an end-to-end solution from research to four pilot production lines to support biologics development and manufacture in the pre-clinical and early clinical stages. R & D equipment investment thus far has been >$20 million dollars. The Mab-Venture team is just over 100 people and is expanding rapidly, with headcount expected to be over 150 by the end of 2017.

In April 2017, Mab-Venture and Thermo Fisher Scientific signed a strategic cooperation and will jointly establish Asia-Pacific’s first antibody drug "SmartFactory", to accelerate the development of biopharmaceuticals. The center will provide a variety of antibody contract development (CRO) and contract manufacturing (CMO) services.

The company's Sr. Management team has over 20 years of biologics R&D experience in various areas including; analytical and bioanalytical R&D, process development, cGMP manufacturing, pre-clinical in vivo studies, antibody discovery, and target validation. Mab-Venture’s Senior Management gained its experience working in academia and multinational biopharma such as Amgen, Novartis, J&J, GSK, Medimmune, Eli Lilly, and other leading global biopharmaceutical companies. We have more than 10 years CRO and customer management experience, and have led 17 integrated research and development projects on behalf of domestic and foreign biopharmaceutical companies.

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Mab-Venture Biopharma has not listed any services.

Analytical Chemistry Services
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Integrated biologics testing capabilities from product characterization to method development/verification/validation to product lot release and stability.

Integrated biologics testing capabilities from product characterization to method development/verification/validation to product lot release and stability.

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Applied Biosystems 7500 Fast Real-Time PCR system
AKTA Pilot
AKTA Avant
Flow Cytometry
MALDI-TOF-MS
HPLC
Agilent 1200
Antibody Screening
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Analytical Method Development
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Full analytical method development from scratch for biologics. Cell-based potency assays included.

Full analytical method development from scratch for biologics. Cell-based potency assays included.

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Drug Development
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Process Consulting
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Upstream/downstream process development services for mammalian cell lines to help achieve a highly stable product with high titer, and >60% recovery.

Upstream/downstream process development services for mammalian cell lines to help achieve a highly stable product with high titer, and >60% recovery.

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Stable Cell Line Generation
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Transient and stable cell line production using ExpiCHO and CHO-K1 platforms respectively. Through an internally developed platform, we offer highly stable CHO cell lines with high titer in just 13 weeks.

Transient and stable cell line production using ExpiCHO and CHO-K1 platforms respectively. Through an internally developed platform, we offer highly stable CHO cell lines with high titer in just 13 weeks.

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CHO
Antibody Manufacturing
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250 L Non-GMP manufacturing using SUBs, with 500L GMP coming online for phase I clinical trials. We are also expanding to 2000L SUBs in 2019.

250 L Non-GMP manufacturing using SUBs, with 500L GMP coming online for phase I clinical trials. We are also expanding to 2000L SUBs in 2019.

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CHO
Bioanalytical Assays
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Detection of combination anti-drug antibodies (ADAs), PK/PD Studies

Detection of combination anti-drug antibodies (ADAs), PK/PD Studies

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Therapeutic Monoclonal Antibody (mAb) Development
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Antibody Services
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Chemistry and Materials
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Biochemistry & Molecular Biology
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Drug Discovery & Development
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Biology
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Bioanalysis
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Protein Services
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Cell and Tissue Culture
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Cells and Tissues
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Pharmacology & Toxicology
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Project Management
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Monoclonal Antibody (mAb) Production
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Antibody Purification
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Antibody Modification
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