Discover Porton Pharma: Our Mission, Values, and Expertise

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    About Us

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

    About Porton

    Porton Pharma Solutions, a global company with R&D, and GMP-compliant manufacturing facilities across US, EU and China, provides customer-centric innovative, and reliable CDMO solutions for Small Molecules, Tides, Biologics and Conjugates (ADCs, AOCs, PDCs, etc.) from pre-clinical to commercial.

      5

      Regulated Markets
      Approval

      4300+

      Global
      Employees

      1200+

      R&D
      Scientists

      2000+

      Total
      Capacity (m³)

      1000+

      Global
      Customers

      3500+

      Milestone
      Projects

    Corporate Culture

      Mission

      Enabling the public's early access to good medicines.

      Vision

      To be the most open, innovative and reliable pharmaceutical service platform in the world.

      Value

      ・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
    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
    Started Shanghai Headquarters, DP Facility in USA, DS Facility in EU (Slovenia), Tides and Conjugates Facility in Shanghai
    2024
    Slovenia Site R&D Facility Operation; Changshou Site Passed USFDA Inspection with Zero 483
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