Neelam Gill advises clients and supports Keller and Heckman Partners in the areas of food and drug law and tobacco ande-vapor law, counseling both domestic and international corporations on product and regulatory compliance issuesinvolving the U.S. Food and Drug Administration (FDA). In her tobacco and e-vapor practice, Neelam advises tobacco, e-cigarette, and e-liquid manufacturers, distributors, retailers,suppliers, and trade associations on FDA, state, and global regulatory compliance issues. In the food and drug arena, sheassists clients with a variety of FDA regulatory matters and labeling issues. Neelam’s background and experience in thepharmaceutical industry serves her well in advising clients on the complexities of the Family Smoking Prevention andTobacco Control Act, in particular with quality systems and good manufacturing practices. Neelam advises clients on preparation of FDA submissions, including premarket tobacco product applications (PMTAs),substantial equivalence (SE) reports, tobacco product master
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