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Deepaben Bhavsar led a flawless IND submission for a CKD drug, achieving FDA approval with zero errors and setting new standards in regulatory excellence.
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Deepaben Bhavsar successfully led the IND submission for a CKD drug, managing 950 CSR documents with exceptional precision and achieving FDA approval without delays or errors. Her strategic planning, quality control, and cross-functional leadership accelerated timelines and set new benchmarks in regulatory excellence, earning her organizational recognition and career advancement.