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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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    District Decision : Voluntary Action Indicated

    Inspection End Date : 2023-02-03

    Dynavax Technologies

    City : Dusseldorf

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    Country/Area : Germany

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    Project Area : Vaccines and Allergenic Products

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2023-02-03

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    District Decision : Voluntary Action Indicated

    Inspection End Date : 2019-03-05

    Dynavax Technologies

    City : Dusseldorf

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    Country/Area : Germany

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    Project Area : Vaccines and Allergenic Products

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2019-03-05

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    FDA Audited

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    District Decision : Voluntary Action Indicated

    Inspection End Date : 2012-10-17

    Dynavax Technologies

    City : Emeryville

    State : California

    Country/Area : U.S.A

    Zip : 94608

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    Project Area : Bioresearch Monitoring

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2012-10-17

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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.