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    HTL Biotechnology is the world leader in the responsible development and production of pharmaceutical-grade biopolymers.

    Send me more info on How To Grow My Business Digitally?

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    01 Compliance, Regulatory & Consulting

    02 Compliance, Regulatory & Consulting

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    01 DZS Clinical Services

    02 Elligo Health Research

    03 Factory CRO

    04 PAREXEL International Corporation

    05 Quotient Sciences

    06 TFS International AB

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    01 Sweden

    02 U.S.A

    03 United Kingdom

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    Quotient Sciences

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    CLINICAL TRIAL DESIGN

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    Quotient Sciences offers modeling & simulations for formulations and clinical designs. Its experts use GastroPlus™ to model biopharmaceutical & PK data, providing valuable insights into the in-vivo performance of molecules & formulations.

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    Pharma Service: Clinical Trials

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    Clinical Trial Design

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    DZS Clinical Services

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      CLINICAL DEVELOPMENT STRATEGY

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      DZS Clinical Services provides expert consultation and advice on the strategic direction of your clinical trial for your drug product or device across many therapeutic areas in the biopharmaceutical, medical device and government and nonprofit sectors.

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      Elligo Health Research

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        GOES DIRECT APPROACH

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        Our team Goes Direct with an approach that redefines the clinical trial process — finding and identifying patients for studies, then providing their physicians with the personnel, processes, technology and infrastructure to conduct them in their own clinics.

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        TFS International AB

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          PROTOCOL DESIGN

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          The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

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          PAREXEL International Corporation

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          SIMPLIFY STUDY DESIGN

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          During study design, it’s critical to to optimize protocol design and global placement to achieve predictable delivery and avoid amendments that slow the process. After all, 55% of trial delays happen at the site level[1], which can have a cascade effect downstream. PAREXEL's ForeSite™

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          Factory CRO

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            PROTOCOL / STUDY DESIGN

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            Our extensive experience and knowledge can help you plan a optimal study design. In addition to our internal expertise, you can get direct market feedback through meetings with panels of clinical experts. Let us be your bridge to the key opinion leaders and surgical experts throughout Europe.

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