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    Lucas Sá

    CMC Project Manager and Pharma R&D

    Lucas Sá is a professional with a strong background in the development of drug products using the Quality by Design (QbD) approach, Design of Experiments (DoE), and Risk Analysis.

    He excels in project management of API and Drug Product projects, with expertise in scale-up, tech transfer, troubleshooting, and process optimization.

    Lucas has comprehensive knowledge of regulatory legislation from EMA, FDA, ANVISA, and WHO, coupled with experience in preparing and reviewing documents for regulatory compliance.

    His skill set includes preformulation and stability studies, as well as physicochemical characterization of API, excipients, and Drug Products using various techniques like DSC, XRD, TGA, DLS, NMR, FTIR, and microscopy.

    Furthermore, he is familiar with manufacturing equipment, which complements his expertise in pharmaceutical industrial technologies.

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    Location

    Germany