CellPort

CellPort provides integrated manufacturing execution and quality management platforms for cell and gene therapy, biologics, and complex regulated manufacturing operations. Driftpin provides strategic consulting and implementation services that align CellPort’s platform with GxP compliance requirements, validation standards, and operational excellence frameworks.

Driftpin Service Alignment:

Fractional Executive Services: Our fractional QA, Risk Management, and Information Security expertise supports CellPort implementations at the strategic level, providing C-suite oversight for manufacturing technology initiatives without full-time executive overhead.

Use Cases:

  • Cell and gene therapy manufacturing execution and quality management
  • Biologics production workflow automation with integrated quality controls
  • Manufacturing data integrity and regulatory compliance documentation
  • Batch record management and deviation tracking across manufacturing operations
  • Supply chain integration with manufacturing execution and quality systems

Why We Partner: CellPort’s manufacturing platform requires systematic implementation planning, validation expertise, and ongoing compliance management that aligns with our data-centric approach to GxP operations. We provide the strategic oversight and systematic methodology needed to ensure successful deployment and sustained regulatory compliance.

Implementation Approach: We document actual manufacturing workflows before system configuration, ensuring CellPort’s platform supports real operational requirements rather than theoretical processes. Our validation methodology focuses on critical data flows and manufacturing dependencies that affect product quality and regulatory compliance.

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