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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 December 31, 2025, Porton has over 4,300 employees globally, has built partnerships with more than 1,400 customers, and has successfully delivered over 5,000 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

    4300+

    Global
    Employees

    1200+

    R&D and TechOps

    ~2200

    Total
    Capacity (m³)

    1400+

    Global
    Customers

    5000+

    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 CMO2005-2008 Became a Public Company2009-2016 Transformed to a Global Leading CDMO2017 to date
Started CMO2005-2008
2005s
2005
Porton Founded
2006
Started CMO (Changshou) With R&D (Chongqing & Chengdu)
2008
Established Porton USA & Europe(Sales), Shanghai (R&D)
Became a Public Company2009-2016
2009s
2013
1st USFDA Inspection With Zero 483
2014
Listed On Shenzhen StockExchange
2015
Acquired the Jiangxi Yichun Plant
Transformed to a Global Leading CDMO2017 to date
2017s
2017
Acquired J-STAR Research Inc. (USA)
2020
Passed EMA Inspection, Started DP CDMO Services
2021
Acquired Hubei Plant (China)
2022
Started DP Commercial Plant Operation; Acquired Fengxian (Shanghai) GMP Plant
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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