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    Looking for Overview? Find Clinical Trials for Compliance, Regulatory & Consulting & other pharma service details on PharmaCompass.

    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 Renejix (1)

    02 Clinica Research Solutions (1)

    03 ICBio Clinical Research Pvt Ltd (1)

    04 Prague Scientific (1)

    05 Reliance Clinical Testing Services, Inc (1)

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    01 Czech Republic (1)

    02 India (2)

    03 U.S.A (2)

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    Renejix

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      Virtual BoothRenejix: CDMO with expertise in small molecule oral dosage, delivery tech, and multi-modality manufacturing.
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      REGULATORY COMPLIANCE

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      Renejix is a CDMO that provides full services for clinical trial supply packaging, labeling, storage, and delivery, assuring regulatory compliance and effective supply chain management.

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      Pharma Service: Clinical Trials

      Category: Compliance, Regulatory & Consulting

      Sub Category: Overview

      Regulatory Compliance

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      Reliance Clinical Testing Services, Inc

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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

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        Prague Scientific

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        REGULATORY SUPPORT

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        From early-stage development through the approval and launch of new products, Prague Scientific's regulatory experts can assist with all regulatory needs across the entire product lifecycle.

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        Pharma Service: Clinical Trials

        Category: Compliance, Regulatory & Consulting

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        Clinica Research Solutions

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          CLINICAL TRIAL REGULATORY SUPPORT

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          CLINICA provides support for drug development partners to overcome hurdles related to clinical requirements of the DCGI, FDA, EMA, & other regulatory authorities. It offers preparation of regulatory packages, CTRI registration, product registration, etc.

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          Pharma Service: Clinical Trials

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          ICBio Clinical Research Pvt Ltd

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          DOSSIER DEVELOPMENT (CTD / ECTD)

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          We do offer Dossier compilation as per Asean Common Technical Dossier (ACTD), Common Technical Dossier (CTD) Guidelines, Drug Master File. We draft data for BMR, MFR, Process & Analytical Validation, Stability Study reports, COA & related reports.

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          Pharma Service: Clinical Trials

          Category: Compliance, Regulatory & Consulting

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