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Company Introduction

Company Introduction

Your Trusted CDMO Partner Accelerating Biologics, Cell & Gene Therapies, and mRNA Innovations.

Who We Are?

ProBio, a subsidiary of GenScript, is a global CDMO offering end-to-end services from discovery to GMP for plasmids,
antibodies, and cell & gene therapies. We bring together multidisciplinary expertise to accelerate development and
manufacturing through customized, and comprehensive services.

ProBio Mission – To be a leading global CDMO enabling life-changing therapies
ProBio provides end‑to‑end CGT support, covering CMC for plasmids, viral vectors, mRNA vaccines, and nucleic acid drugs, from IND filing through clinical and commercial manufacturing. Our integrated CMC services span cell banking, process development, characterization and validation, analytical development, and stability studies.
We also offer innovative biologics discovery and development capabilities, including antibody discovery, engineering, and in vitro/in vivo pharmacology. ProBio delivers a full DNA‑to‑GMP platform with stable cell line development, host cell licensing, process and analytical development, and clinical to commercial manufacturing.
ProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017.

We have established GMP capacity meeting the regulatory requirements of the US Food and Drug Administration (FDA), European Medicines Agency (EMA) and National Medical Products Administration (NMPA).

ProBio End-to-End CGT Support – Over 150 IND Approvals Since 2017
ProBio operates a growing global network of development and manufacturing facilities to support U.S. and international programs.
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United States

Hopewell, New Jersey — A U.S.-based Cell & Gene Therapy Center of Excellence specializing in plasmid DNA and viral vector development and GMP manufacturing. The Hopewell site is designed to meet FDA regulatory expectations and support close collaboration with U.S. clients.
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China (CN)

Multiple sites supporting discovery, development, and GMP manufacturing across modalities. Our global footprint enables proximity to customers, alignment with regional regulatory requirements, and reliable supply across key markets.
Proven Quality & Credibility
Proven Quality & Credibility
cGMP-compliant facilities aligned with global regulatory standards (FDA, EMA, NMPA)
Proven Quality & Credibility
Experience supporting programs from early development through commercial supply
Proven Quality & Credibility
Trusted partner to biotech and biopharma companies worldwide
Proven Quality & Credibility
Dedicated modality-focused teams and purpose-built facilities

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