Prashant Choudhari

Experience

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  Neon Laboratories Limited

  Jul 2022 - Mar 2024

  Formulation & Development

  • Practice of Literature search, Patent search, Data compilation, Data analysis, Preformulation studies, Innovator sample evaluation.• Preparation of documents such as Stability protocol, Product Development Report (PDR), Trial Batch Reports (TBR), Bill of Material (BOM), Master formula records (MFR).• Knowledge of manufacturing documents like Batch Manufacturing Records (BMR), Specifications, Analytical Methods, Stability Data• Resolving regulatory query, To review Artwork and Data Sheets (DS).• Knowledge of Clinical Trial Phases, Product Development and Drug Development Process, Acquainted with ICH Guidelines,• To Prepare and perform Hold time study protocol, In use study protocol, Compatibility study protocol and report for the same. • To Execute Trials, Stress batches & Stability batches of different formulations of Tablets, Capsules and Injections.• Compilation of trial details, Stability reports. Show less

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  IDRS LABS PRIVATE LIMITED

  Mar 2024 - now

  Research associate