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    Pharma Services Category of Dalmia

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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 BioAnalytical Services (2)

    02 Clinical Development / Phase IIb-IV (3)

    03 Compliance, Regulatory & Consulting (2)

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    01 Dalmia (7)

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    01 India (7)

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    Dalmia

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      BIOAVAILABILITY / BIOEQUIVALENCE STUDIES

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      We deliver the Bioavailability/ Bioequivalence study projects with high quality standards as per the set regulatory guidelines to ensure the efficacy and safety of each pharmaceutical products.

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      Pharma Service: Clinical Trials

      Category: Clinical Development / Phase IIb-IV

      Sub Category: Bioavailability / Bioequivalence
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        REGULATORY AFFAIRS

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        DRDL is providing an effective strategy of Pharmaceutical APIs, Finished Formulation and New medical device registration in India with the help of our network partner in the segment.

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        Pharma Service: Clinical Trials

        Category: Compliance, Regulatory & Consulting

        Sub Category: Regulatory Affairs
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          PHASE II & PHASE III CLINICAL TRIALS

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          We provide end to end services on clinical trial: Early Phase Trials – Phase I & Phase II, Late Phase Trials - Phase III & Phase IV. We are providing solutions for Early & Late Phases trials with our hospital network across India & abroad.

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          Pharma Service: Clinical Trials

          Category: Clinical Development / Phase IIb-IV

          Sub Category: Phase II / III
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            PHASE IV CLINICAL TRIAL

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            We provide end to end services on clinical trial: Early Phase Trials – Phase I & Phase II, Late Phase Trials - Phase III & Phase IV. We are providing solutions for Early & Late Phases trials with our hospital network across India & abroad.

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            Pharma Service: Clinical Trials

            Category: Clinical Development / Phase IIb-IV

            Sub Category: Phase IV
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              MEDICAL DEVICES

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              Launch your Medical Device in the market with DRDL. We have built the absolute roadmap by keeping in view the FDA, EMA and other necessary regulations. Where, we are keeping a top view on the data monitoring, safety and risk-management.

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              Pharma Service: Clinical Trials

              Category: Compliance, Regulatory & Consulting

              Sub Category: Medical Devices
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                BIOANALYTICAL SERVICES

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                We have a dedicated team on the platform to connect for the requirements & execute the project ahead of timeline. We are meeting all the current standards of the Good Clinical Practices (GCP) & Good Laboratory Practices (GLP).

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                Pharma Service: Analytical

                Category: BioAnalytical Services

                Sub Category: Overview
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                  PRE-CLINICAL TESTING SERVICES

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                  At DRDL, we are equipped with the excellent expertise & chains of value with the vast network strength to deliver fast research, pre-clinical testing & regulatory approval to end up with the effective drug molecule & medical devices.

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                  Pharma Service: Analytical

                  Category: BioAnalytical Services

                  Sub Category: Bioequivalence / Clinical / Pre-Clinical Testing
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