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    Pharma Services Category of CRMO Pharmmatecch

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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 Contract Manufacturing (1)

    02 Custom Synthesis & Manufacturing (1)

    03 GMP Manufacturing (1)

    04 Regulatory Affairs / Pharmacovigilance (2)

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    01 CRMO Pharmmatecch (5)

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    01 India (5)

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    CRMO Pharmmatecch

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      CONTRACT MANUFACTURING OUTSOURCING

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      - Service Details

      CRMO has successfully catered to diverse pharmaceutical outsourcing requirements of number of European, US and Japanese customers because of the in depth knowledge of the Indian pharmaceutical industry and sound understanding of outsourcing trends.

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      Pharma Service: API Manufacturing

      Category: Contract Manufacturing

      Sub Category: Overview
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        GMP MANUFACTURING CONSULTING

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        CRMO offers consulting services covering Current Good Manufacturing Practices(cGMP), Quality Management including all aspects of Good Laboratory Practice(GLP), Validation and Qualification as well Regulatory agency Documentation.

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        Pharma Service: API Manufacturing

        Category: GMP Manufacturing

        Sub Category: Overview
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          CUSTOM MANUFACTURING PROJECT EXECUTION

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          CRMO Pharmmatecch will ensure execution of the entire custom-manufacturing project on behalf of the customer.

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          Pharma Service: API Manufacturing

          Category: Custom Synthesis & Manufacturing

          Sub Category: Custom Synthesis
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            REGULATORY SUPPORT - INDIA

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            CRMO can assist your company with FDA pre and post approval inspections, regulatory interpretation & submissions such as DMFs to the US FDA & EU Community, Dossiers for Certificate of Suitability of monographs of the European Pharmacopoeia, etc

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            Pharma Service: Sales, Marketing, Registration

            Category: Regulatory Affairs / Pharmacovigilance

            Sub Category: India
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              REGULATORY SUPPORT - US

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              - Service Details

              CRMO can assist your company with FDA pre and post approval inspections, regulatory interpretation & submissions such as DMFs to the US FDA & EU Community, Dossiers for Certificate of Suitability of monographs of the European Pharmacopoeia, etc

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              Pharma Service: Sales, Marketing, Registration

              Category: Regulatory Affairs / Pharmacovigilance

              Sub Category: United States
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