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Purva Shah is a pharmaceutical regulatory affairs professional with a strong foundation in dossier preparation, quality control, and international compliance. With hands-on experience at leading pharma companies like Intas Pharmaceuticals and Tasmed (India), she has successfully managed regulatory submissions for over 50 pharmaceutical and nutraceutical products across 15+ African and Asian markets, including jurisdictions like TFDA, NMRA, HSA, and MOH.

Her expertise spans CTD/ACTD dossier compilation, labeling compliance, export documentation, and regulatory query resolution. Purva’s scientific precision and market-specific knowledge now power her independent consultancy, specializing in helping companies navigate the complex regulatory landscapes of emerging markets in Africa and Asia.

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TheApostrophe

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