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BLA

BLA

Process Characterization and Process Validation

Core Advantage

As an important link of pharmaceutical research and a prerequisite for the registration of a product for marketing approval, Process characterization (PC) and process validation (PV) studies aim to ensure that the drug manufacturing process is always under control and can consistently produce products that meets quality requirements.

  • Rigorous Method Design

    Process validation and continuous lifecycle management are based on the internationally accepted "Quality by Design" (QbD) concept and the rigorous DoE design test method. The protocol is designed in strict accordance with the regulatory requirements (NMPA/FDA/EMA) of the region where the investigational drug need to obtain the approval and marketing authorization.

  • Flexible solutions

    Customized solutions can be made for clients with specific needs and at specific stages of their projects. Flexible scheduling and multiple parallel lines can be guaranteed to shorten the project cycle.

  • Experienced technical team

    The advanced process, strong production team, and rich practical experience in PC/PV programs ensure smooth project delivery.

Service Content

Process Characterization
  • Process scale down modeling
  • Upstream and downstream and formulation process characterization studies
  • Studies on purification packing and membrane package filtration life
  • Critical process parameter assessment/risk assessment
  • Storage stability study of culture media
  • Purification impurity challenge study
Process Validation
  • PV bulks and preparation production (3*2000L stock solution bulks and formulation production, UPB and EOPC preparation, synchronized 3L upstream satellite tank)
  • Material compatibility studies
  • Stability study
  • Method validation
  • Process validation batch protein characterization study
  • Shipping validation

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BLA

BLA

Process Characterization and Process Validation

Core Advantage

As an important link of pharmaceutical research and a prerequisite for the registration of a product for marketing approval, Process characterization (PC) and process validation (PV) studies aim to ensure that the drug manufacturing process is always under control and can consistently produce products that meets quality requirements.

  • Rigorous Method Design

    Process validation and continuous lifecycle management are based on the internationally accepted "Quality by Design" (QbD) concept and the rigorous DoE design test method. The protocol is designed in strict accordance with the regulatory requirements (NMPA/FDA/EMA) of the region where the investigational drug need to obtain the approval and marketing authorization.

  • Flexible solutions

    Customized solutions can be made for clients with specific needs and at specific stages of their projects. Flexible scheduling and multiple parallel lines can be guaranteed to shorten the project cycle.

  • Experienced technical team

    The advanced process, strong production team, and rich practical experience in PC/PV programs ensure smooth project delivery.

Service Content

Process Characterization
  • Process scale down modeling
  • Critical process parameter assessment/risk assessment
  • Upstream and downstream and formulation process characterization studies
  • Storage stability study of culture media
  • Studies on purification packing and membrane package filtration life
  • Purification impurity challenge study
Process Validation
  • PV bulks and preparation production (3*2000L stock solution bulks and formulation production, UPB and EOPC preparation, synchronized 3L upstream satellite tank)
  • Method validation
  • Material compatibility studies
  • Process validation batch protein characterization study
  • Stability study
  • Shipping validation