The Office of Management and Budget recently approved, without any changes, the Federal Trade Commission’s (FTC) proposed study of authorized generic pharmaceutical drugs. Through this study, the FTC will analyze aspects of competition between brand-name and generic drugs. This webinar will provide insight into the issues of interest and information that the FTC will subpoena for the FTC’s study, including how a company can protect its confidential business information if subpoenaed by the FTC. Ms. DeSanti also will discuss comparisons of the FTC's authorized generics study with past studies conducted by the FTC in 2002 and 2005. Click here for more information on the event.