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blue inspection

helps you to ensure compliance
in your pharmaceutical supply chain.

Dedicated to excellence:

The audits you require are performed to the highest level of quality, independence and integrity.

blue inspection, with more than 15 years’ experience, is a leading provider of GxP audits worldwide and is accredited according to ISO 17020 for performing audits at API and excipient manufacturers.

Team

blue inspection - Dr. Maja Frommeyer
blue inspection - Dr. Marvin Gohrbandt
blue inspection - Dr. Nicole Hübel
blue inspection - Dr. Thilo Sandner
blue inspection - Dr. Gabriele Siedenburg
blue inspection - Dr. Kerstin Tabatt
blue inspection - Dr. Norbert Waldöfner

    Our long-term expertise in GxP Auditing
    include the following audits:

    APIs

    The suppliers of active pharmaceutical ingredients need to audited at least every three years to ensure GMP compliance.

    Excipients

    An audit of your excipient supplier can ensure that appropriate good manufacturing practices are met, based on a formalized risk-assessment.

    Packaging Materials

    Audits at packaging material suppliers for pharmaceutical products can ensure compliance with applicable GMP requirements, especially for primary, sterile and printed packaging materials.

    Contract Manufacturer / Lab Audits

    As an essential requirement for the release of medicinal products to the market, regular audits of CMOs and laboratories are important to ensure GMP compliance.

    GDP audits

    Companies involved in the distribution of pharmaceutical products need to undergo regular assessment. An audit according to Good Distribution Practice assesses compliance surrounding the logistics for pharmaceutical products.
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    Phone: +49 251 284 972 93
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    +49 251 284 972 93
    blue inspection

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