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Smarter Trials Through Strategic Guidance

Clinical trials rely on more than logistics. They require foresight, alignment, and precision planning. Our CT Consulting services help you optimize trial design, regulatory pathways, and supply strategies without adding complexity. From demand forecasting and protocol review to Importer of Record support and QA guidance, we support your trial’s success from the earliest planning phases onward.

Every clinical trial is different, and effective execution starts long before materials are moved. Our CT Consulting services bridge the gap between protocol and practice. Whether you are designing a first-in-human study, managing hospital-led IITs, or scaling a multi-site program, we help translate clinical intent into practical supply chain solutions. With decades of experience and a trial-centric mindset, our experts deliver insights, foresight, and clarity. From demand forecasting to regulatory navigation, we empower sponsors with the confidence to move forward.

About CT Consulting

Translating a clinical protocol into reality requires more than operational capabilities. It requires insight. Our CT Consulting services provide early-phase planning, protocol alignment, and regulatory guidance tailored to your trial’s scale, setting, and complexity. We specialize in helping biotech firms, academic institutions, and healthcare providers streamline their study planning while staying compliant, cost-conscious, and timeline-focused.

  • Protocol-to-Practice Supply Planning

    We translate clinical protocols into executable supply strategies. This includes kit design, country adaptations, and scenario planning for real-world trial execution.

  • Demand Forecasting & Waste Mitigation

    Volume modeling aligned with recruitment dynamics helps optimize batch sizes, reduce overage, and support timely availability without excess.

  • Regulatory Navigation & IOR Handling

    Support for import and export compliance, QP release coordination, and Importer of Record setup. Tailored to decentralized or non-commercial trial settings.

  • Site Readiness & Local Enablement

    Strategic support for site onboarding, logistics coordination, and regional regulatory alignment. Well suited to hospital-initiated or investigator-led trials.

  • Integrated QA Insight & Audit Preparation

    Trial-specific guidance across documentation flow, GxP readiness, and QA best practices to support smoother inspections and operational integrity.

Why Komtur

  • Flexible Comparator Sourcing

    A broad supplier network and hybrid sourcing strategies ensure compliant, reliable, on-schedule supply. This is backed by long-standing, trusted relationships.

  • Agile Distribution with Local Execution

    GDP- and GMP-compliant operations across 18 affiliates enable scalable logistics and direct-to-site delivery in complex trial settings.

  • Tailored Packaging and Labeling

    Custom small-batch packaging and multilingual labeling. Adapted to timelines, protocols, and country-specific requirements.

  • A Heritage of Sponsor Trust

    Decades of experience in clinical supply, supporting biotech, big pharma and investigators with precision, reliability, and global coordination.

  • Regulatory & Strategic Support

    Guidance across QP release, IOR services, and import/export compliance. These safeguards ensure control, speed, and seamless execution.

“Komtur’s CT Consulting provided invaluable support, allowing us to align complex trial logistics with regulatory requirements across multiple regions.”