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Snehal Trivedi

Snehal Trivedi focuses her practice on U.S. Food and Drug Administration (FDA) policy and regulatory matters and advises food manufacturers and pharmaceutical clients in preparing FDA correspondences and other post-market filings. She draws upon 10 years of pharmaceutical industry experience and has drafted and negotiated various license, distribution, and clinical trial agreements on behalf of leading pharmaceutical companies, contract research organizations and university hospitals. Snehal has experience in facilitating due diligence efforts related to state boards of pharmacy laws and regulations related to prescription drugs and controlled substances.