
Michael Chappell’s extensive FDA experience brings a unique understanding of how regulated industry is impacted by FDA’s enforcement operations. Chappell joins Greenleaf following a distinguished 38-year career in FDA’s Office of Regulatory Affairs where he most recently served as head of the agency’s Office of Regulatory Affairs.
In his new role, Michael will serve as a Senior Advisor and will work with Greenleaf clients to provide strategic consulting services on regulatory, enforcement and compliance matters.
Prior to joining Greenleaf, Chappell served as FDA’s Acting Associate Commissioner for Regulatory Affairs and Deputy Associate Commissioner for Field Operations from 2007 – 2010. In this role, he was head of a 4,000-person staff spanning five regional offices that are responsible for imports, inspections and enforcement policy.
Previously, Chappell served as director of the Dallas District where he was responsible for all FDA domestic field activities in Texas, Oklahoma and Arkansas. He was also a supervisory consumer safety officer in the Atlanta District and a director of investigations for the Florida District, where he managed all field investigational programs for the district and one of the largest import operations in FDA’s Southeast Region.
Mr. Chappell started his FDA career as a consumer safety officer in Nashville. He later became the resident in charge of the Memphis Resident Post of the Nashville District, where he was responsible for new emphasis programs for the field force in medical devices, biologics, and bioresearch. Mr. Chappell is a graduate of the University of Alabama.