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    Pharma Services Category of Quorum Review, Inc.

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    HTL Biotechnology is the world leader in the responsible development and production of pharmaceutical-grade biopolymers.
    Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
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    01 Compliance, Regulatory & Consulting (2)

    02 Patient / Investigator Recruitment (1)

    03 Technology / Data / Analytics (1)

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    01 Quorum Review, Inc. (4)

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    01 U.S.A (4)

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    Quorum Review, Inc.

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    DEVICE STUDIES

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    Quorum understands the complexities of device research. Our boards have extensive experience with devices, our regulatory team can help determine the appropriate classifications for your product, and our support staff can guide you through the particulars of reviewing device research.

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    Pharma Service: Clinical Trials

    Category: Compliance, Regulatory & Consulting

    Sub Category: Medical Devices
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    COMBINATION PRODUCT STUDIES

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    Quorum has extensive experience with combination products. Our boards and regulatory teams understand the intricacies of combination product research. We can help determine the correct way to manage your study, and we will apply the proper standards for your product.

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    Pharma Service: Clinical Trials

    Category: Compliance, Regulatory & Consulting

    Sub Category: Medical Devices
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    INFORMED CONSENT FOR THE 21ST CENTURY

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    Imagine an eConsent solution that improves compliance and consent accuracy and provides an IRB-integrated process that activates studies in days instead of weeks. Q Consent is the future of electronic informed consent and it’s available now for your research studies.

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    Pharma Service: Clinical Trials

    Category: Patient / Investigator Recruitment

    Sub Category: Patient Recruitment
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    ONQ PORTAL- TRACK YOUR STUDY

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    The OnQ Portal™ helps you track your study through the IRB review process, from submission to approval documents

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    Pharma Service: Clinical Trials

    Category: Technology / Data / Analytics

    Sub Category: Clinical Trial Monitoring
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