Integrated Biosimilar CMC Solutions – from Development to Commercial Manufacturing

Integrated Biosimilar CMC Solutions – from Development to Commercial Manufacturing
Product Description

End‑to‑end biosimilar development from cell line construction to PPQ and commercial batches. The integrated platform enables a fast development timeline, supports global GMP requirements, and offers competitive cost of goods. Includes DS/DP manufacturing, analytical testing, quality support, and technology transfer.

Canton Biologics

  • Country/Region:
    Hong Kong
  • Founded:
    2016
  • On CPHI since:
    2026
  • Employees:
    250 - 499
Company types
CMO/CDMO
Specifications
  • CAS Registry Number
    N/A
  • Details
    Full CMC services including cell line development, upstream/downstream process development, analytical development, process characterization, technology transfer, process validation (PPQ), and commercial manufacturing; compliant with NMPA, FDA, and EMA GMP, with EU QP release support.

  • Selling Points
    Fully integrated services from cell line to commercial batch, reducing outsourcing risks and project complexity.

  • Model
    Integrated development model with accelerated timeline
  • Supplied from
    China
  • Measured In
    Container

Canton Biologics

  • Country/Region:
    Hong Kong
  • Founded:
    2016
  • On CPHI since:
    2026
  • Employees:
    250 - 499
Company types
CMO/CDMO

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