Covington offers one of the most comprehensive life sciences industry-focused practices with more than 250 lawyers across multiple offices worldwide advising drug, biologics and device companies on FDA regulatory, healthcare, government contracts, corporate, IP, public policy and trade issues. Players in the health care field turn to Covington because they recognize that navigating government regulation is fundamental to their success, and that Covington offers unique expertise across a number of practices and works collaboratively to apply that expertise to client needs. Covington regularly advises clients about compliance, risk management and strategy with regard to participation in Medicare, Medicaid and 340B, as well as development and procurement agreements with government agencies.