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About Us

A Customer-centric, Innovative
and Reliable CDMO with Global Solutions

About Porton

Founded in 2005, Porton Pharma Solutions provides end-to-end, customized R&D and GMP manufacturing services to pharmaceutical and biotech companies, as well as research institutions worldwide, spanning the entire drug lifecycle from pre-clinical development to commercialization. Our capabilities cover both drug substances (APIs) and drug products across multiple modalities, including Small Molecules, TIDES, Biologics and Conjugates (ADCs, AOCs, DACs, PDCs, RDCs, etc.), and Advanced Therapy Medicinal Products. As of June 30, 2026, Porton had over 4,400 employees globally, built partnerships with more than 1,500 customers, and successfully delivered approximately 6,000 projects. We are committed to a customer-centric approach, delivering innovative and reliable global CDMO solutions, enabling earlier access to good medicines.


    5

    Regulated Markets
    Approval

    4,400+

    Global
    Employees

    1,200+

    R&D and TechOps

    ~2,200

    Total
    Capacity (m³)

    1,500+

    Global
    Customers

    ~6,000+

    Milestone
    Projects

Corporate Culture

    Mission & Vision

    Enabling Earlier Access to Good Medicines

    Values

    ・Customers First
    ・Teamwork
    ・Efficient Execution
    ・Embrace Changes
    ・Pursuit of Excellence

Our Journey to Excellence

Started CMO2005 to 2009 Listed as a Public Company2010 to 2016 Transformed into an End- to-end CDMO2017 to 2022 Expanded to All Modalities Becoming a Global Leading CDMO2023 to Present
Started CMO2005 to 2009
2005s
2005
Porton Founded
2006
Commissioned the Changshou API Plant and Chongqing R&D Center
2008
Established Porton US and European Offices, and Shanghai R&D Center
Listed as a Public Company2010 to 2016
2010 to 2016
2013
First FDA Inspection with Zero 483
2014
Listed on the Shenzhen Stock Exchange
2015
Acquired the Jiangxi Yichun Plant
Transformed into an End- to-end CDMO2017 to 2022
2017 to 2022
2017
Acquired J-STAR Research Inc. (USA)
2018
Launched Cell & Gene Therapy CDMO
2019
Passed EMA Inspection, Started DP CDMO
2021
Acquired the Hubei Xiaogan Plant
2022
Launched the Chongqing Drug Product (DP) Commercial Plant, Acquired the Shanghai Fengxian Plant
Expanded to All Modalities Becoming a Global Leading CDMO2023 to Present
2023
New Jersey (USA) Facility Capacity Expansion; TIDES, Biologics and Conjugates Facilities Put into Operation
2024
Chongqing Changshou Site Passed FDA Inspection with Zero 483
2025
New Jersey (USA) HPAPI GMP Suite Expansion
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By clicking “Subscribe,” you acknowledge that you have read and agree to our Legal Disclaimer, Terms of Use, and Privacy & Cookie Policy. Porton will use the contact information you provide to communicate with you about our products, services, and other relevant updates. You may unsubscribe at any time. For more information about how we protect your privacy and manage your communication preferences, please review our Privacy & Cookie Policy.

ⓒ 2026 PORTON Legal Notices | Porton Privacy

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