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    Pharma Services Category of Reliance Clinical Testing Services, 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 Clinical Development / Phase IIb-IV (2)

    02 Compliance, Regulatory & Consulting (2)

    03 Patient / Investigator Recruitment (1)

    04 Technology / Data / Analytics (2)

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    01 Reliance Clinical Testing Services, Inc (7)

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    01 U.S.A (7)

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    Reliance Clinical Testing Services, Inc

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      HUMAN REPEAT INSULT PATCH TEST (HRIPT)

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      To determine the safety of topical products, RCTS provides a range of clinical testing procedures, including a broad range of in-use and patch studies. Human repeat insult patch tests (HRIPT) for contact sensitization/irritation and acute or cumulative patch tests irritation.

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      Pharma Service: Clinical Trials

      Category: Clinical Development / Phase IIb-IV

      Sub Category: Phase II / III
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        SAFETY-IN-USE (SIU) STUDIES

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        To determine the safety of topical products, RCTS provides a range of clinical testing procedures, including a broad range of in-use and patch studies. Determining product safety under normal or exaggerated use conditions.

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        Pharma Service: Clinical Trials

        Category: Patient / Investigator Recruitment

        Sub Category: Patient Recruitment
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          CLAIMS SUBSTANTIATION & EFFICACY TESTING

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          Claims substantiation plays a key role in a product’s success and helps ensure the product stands out against competitors. From moisturization and barrier function, to anti-aging and color changes, rely on RCTS for your product claims substantiation and efficacy testing needs.

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          Pharma Service: Clinical Trials

          Category: Clinical Development / Phase IIb-IV

          Sub Category: Bioavailability / Bioequivalence
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            PROTOCOL DESIGN

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            RCTS designs protocols in adherence with International Conference of Harmonization (ICH) and good clinical practice (GCP) guidelines, The research protocol describes in detail how the clinical trial will be conducted.

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            Pharma Service: Clinical Trials

            Category: Compliance, Regulatory & Consulting

            Sub Category: Overview
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              CLINICAL DATA MANAGEMENT

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              The data management process is one of the hallmarks of RCTS. Your data is never unattended as it moves through our system, and sign-off forms are required at every step to ensure complete accuracy.

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              Pharma Service: Clinical Trials

              Category: Technology / Data / Analytics

              Sub Category: Overview
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                ELECTRONIC DATA CAPTURE & ELECTRONIC CASE REPORT FORMS

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                More and more clinical trials are moving toward electronic data capture (EDC) for source documents and CRFs, particularly for pharmaceutical trials. RCTS has worked with EDC systems of several pharmaceutical companies.

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                Pharma Service: Clinical Trials

                Category: Technology / Data / Analytics

                Sub Category: Data Management
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                  PHARMACEUTICAL & MEDICAL DEVICE TESTING

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                  RCTS offers complete clinical testing services for topical drugs and medical devices. Our team has extensive experience in the design and execution of protocols to support the safety and therapeutic benefits of topical drugs and devices across numerous therapeutic areas.

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                  Pharma Service: Clinical Trials

                  Category: Compliance, Regulatory & Consulting

                  Sub Category: Medical Devices
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