AMPLEXOR Webinar on demand desktop-monitor.png

Addressing Regulatory and Compliance Risks : During the Product Launch Pre-Approval Period

Since 2003 when the Office of Inspector General (OIG) of the Department of Health and Human Services first issued its guidance to pharmaceutical manufacturers outlining the basic requirements of an effective compliance program, research-based companies have had to continue to focus on a myriad of activities that required careful compliance, legal and regulatory review.

In this two-part webinar program addressing issues facing pharmaceutical companies, Howard Dorfman, an industry authority with more than 40 years’ experience in healthcare compliance and regulatory oversight, will provide an analysis of pre-approval industry activities that present increased risk to companies even before a product enters the market. The webinar will identify various processes and procedures that impact corporate behavior during this critical period, including interactions with HCPs and the need to present accurate data to a variety of audiences and thereby avoid misstating results of studies that can present potential risks.

Watch now for free

Meet the speaker

Dorfman_Bio Pic-1.jpg

Howard Dorfman is an expert in FDA regulatory law, fraud and abuse, compliance programs, and risk management procedures.  Formerly editor-in-chief and contributing author of the Practicing Law Institute’s Answer Book on Pharmaceutical Compliance and Enforcement, and a Visiting Distinguished Professor at Seton Hall Law School, Howard served as Senior Vice President and General Counsel at Turing Pharmaceuticals; Vice President and General Counsel at Ferring Pharmaceuticals, Inc., and Vice President Assistant General Counsel at Bayer Pharmaceuticals (U.S.).