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Neelam Gill practices in the areas of Food and Drug and Tobacco and E-Vapor law, counseling both domestic and international corporations on product compliance issues involving the U.S. Food and Drug Administration (FDA). In her Tobacco and E-Vapor practice, Ms. Gill 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 arena, she assists food industry clients with a variety of FDA regulatory matters and labeling issues.
Prior to joining Keller and Heckman, Ms. Gill practiced FDA, life sciences, and consumer products regulatory law, representing clients in the food, cosmetic, drug, device, and tobacco sectors. She also has extensive experience in the pharmaceutical industry, where her work involved quality systems, cGMPs, SOPs, product filings, regulatory inspections, product certification and testing, internal compliance programs, risk management, supply chain management, and other areas of FDA compliance. Ms. Gill now draws from her industry knowledge and experience to assist clients with compliance and business concerns specific to FDA-regulated industry.