We assist startups in designing and optimizing GXP-compliant facilities, from initial design to commissioning and validation, ensuring scalability for international markets and supporting local manufacturing initiatives.

Facility Planning & Execution

We provide full-spectrum support from initial concept through execution, ensuring your facility is compliant, scalable, and ready for production.

  • Facility Optimization

    Create efficient, GMP-compliant layouts tailored to your product and scale.

  • Validation

    Ensure all systems perform as intended through documented qualification processes.

  • Tech Transfer Support

    Seamlessly integrate processes from R&D to manufacturing scale.

  • Scale-Up Readiness

    Design with flexibility to support future capacity expansion.

Facility Planning & Execution

Specialized Facility Solutions

We provide end-to-end support, from conceptual design to commissioning and validation, for the following types of facilities:

  • Biopharma Production Facilities
    We design and validate facilities for biologics like monoclonal antibodies, cell therapies, and recombinant proteins. Our solutions ensure GMP compliance and large-scale, high-quality production readiness.
  • Vaccine Manufacturing Facilities
    From pilot plants to full-scale vaccine operations, our facilities meet WHO and GMP standards while supporting modern technologies like mRNA and viral vector platforms.
  • Clinical Testing Centres
    We help establish compliant centers for clinical trials and pharmaceutical testing, tailored for accuracy, patient safety, and regulatory excellence.
  • Bioequivalence Centres
    We design and validate facilities to conduct bioequivalence studies that prove the safety and efficacy of generic medicines, aligned with global regulatory expectations.

 

Your Facility Journey – Answered

Startups planning GMP manufacturing, clinical testing, or vaccine production benefit most from early facility strategy and regulatory design alignment.

Timelines vary, but we streamline commissioning and qualification phases to ensure compliance and reduce delays with a tailored validation master plan.

Yes, our scalable designs allow phased expansions, ensuring that facilities evolve alongside your production capacity and market needs.