5/5 Stars
Managing samples and testing of Small Molecules to Biologics and Vaccines in all stages of development (GMP and non-GMP). Includes drug substance, drug product, raw materials in Stability studies, Release testing and CoA generation, Characterization and some In-process testing. Data standardization in LIMS enables us to produce data tables (in Common Technical Document format) using SAS for regulatory submissions (validated process).
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