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    European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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    Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.

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    USP reference standards; highly characterized specimens of drug substances, impurities, excipients, degradation products & more.

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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.

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    Guizhou Utide Biotechnology Co., Ltd. - Specialized GMP manufacturing for next-generation GLP-1 peptide APIs.

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    Novoprotein

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    Novoprotein Scientific (heze) Inc

    U.S.A
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    Rare Disease Summit
    Not Confirmed

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 38410

    Submission : 2023-05-19

    Status : Active

    Type : II

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    Looking for Drug Master Files (DMF) for 38410 of Novoprotein Scientific (heze) Inc

    Looking for Drug Master Files (DMF) for 38410 of Novoprotein Scientific (heze) Inc 1

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    Novoprotein Scientific (heze) Inc, based in U.S.A, is a pharmaceutical company.

    One of their notable products is RNASE INHIBITOR, GMP GRADE, with a corresponding US DMF Number 38410.

    Remarkably, this DMF maintains an Active status since its submission on May 19, 2023, highlighting commitment to regulatory compliance.

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.