Vitrian serves your entire biopharm construction need by providing a best-in-class, end-to-end solution. From pre-construction, to construction, to fit out and commissioning, Vitrian is the ideal partner to address typically outsourced gaps in the project delivery chain with a streamlined process throughout the entire manufacturing cycle—often occurring concurrently—to speed your product to market.

Upstream Predevelopment
  • Design phase for facilities & company fit-out
  • Assist companies and stakeholders with pre-construction activities:
    • Site selection
    • Project planning
    • Conceptual design
    • Equipment procurement
    • Staffing
Midstream Core & Shell Construction
  • Turnkey project management of core-and-shell facility construction:
    • Consultant coordination and retention
    • Design review
    • Construction management
Downstream Fit-out & Commissioning
  • Bespoke services unique to the CGMP industry:
    • Equipment procurement and testing
    • Fit-out
    • Pre-clinical/early clinical manufacturing
    • Commissioning, qualification, and validation (CQV) for FDA approval

Through the entire manufacturing cycle, Vitrian offers advisory services to clients/users on a fee-for service basis. These services are contracted directly with your company to enhance ROI for your core business.


Our strategic partnerships provide further expertise through all phases of the manufacturing cycle.

  • cGMPnow
    • Assists in upstream with conceptual design and equipment procurement/ staffing, and downstream with FDA approval (CQV).
    • Consulting practice with over 25 years of biopharma and manufacturing experience.
    • Market leader in conceptual design, equipment procurement, automation controls, and CQV.
  • Evolve
    • Assists in upstream with conceptual design and equipment procurement/ staffing.
    • Consulting practice led by former VP of Global Engineering at Catalent.
    • Fee for service owner’s representation, due diligence, and strategic services on behalf of Vitrian or its clients.
    • “In-house” project management augmenting Vitrian’s existing team.
  • Azzur Group
    • Assists in downstream with pre-clinical/early clinical manufacturing and FDA approval (CQV).
    • Operator of Clean Rooms on Demand offering fully serviced clean rooms on a short-term basis for early stage companies.
    • Refers drug development companies and CDMOs that “graduate” from their network and need permanent manufacturing facilities to Vitrian.


For inquiries or more information, contact us at 240.396.1414
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