About
I am a pharmaceutical professional with one year of industry experience in Formulation & Development, where I worked on pre-formulation studies, excipient compatibility, prototype development, QbD-oriented optimization, and CMC-aligned technical documentation. I am particularly interested in the CMC aspects of Regulatory Affairs, including dossier preparation, regulatory strategy, lifecycle management, and quality systems. I enjoy bridging scientific data with regulatory requirements to support compliant, structured, and well-reasoned decision-making.
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