Schevon Salmon is admitted to practice in the District of Columbia and Pennsylvania. He is not currently admitted in North Carolina.
Schevon Salmon is counsel and a member of the Health Care and FDA practice. His practice focuses on counseling companies through the development and manufacturing of pharmaceuticals, biologics, and medical devices at all stages of the product lifecycle. He advises clients on a variety of FDA regulatory and corporate transaction matters, including product development, advertising and promotion, medical communications, good manufacturing practices (drugs and medical devices), and negotiating quality and supply agreements.
Prior to joining the firm, Schevon was a director, corporate counsel at a global pharmaceutical company, where he focused on providing strategic and risked-based guidance to internal stakeholders on a variety of legal, regulatory, and compliance issues related to product development, manufacturing, and promotional activities. Through this role, he collaborated with senior leaders, subject matter experts, and cross-functional teams to develop and implement solutions and accomplish enterprise-wide business initiatives.
