Events | 2016.09.22
FDAnews Announces — False Claims Act Liability for Regulatory Noncompliance: An Update for Drug and Device Manufacturers Webinar, Oct. 19, 2016
How can violations of FDA requirements for promotion and marketing, adverse event reporting or cGMPs trigger the False Claims Act (FCA)? Join Anna Laakmann, Counsel, Greenberg Traurig, on Oct. 19 for the False Claims Act Liability for Noncompliance webinar when she’ll explain how regulatory noncompliance can form the basis of an FCA enforcement action by the government.
(PRWeb September 22, 2016)
Read the full story at http://www.prweb.com/releases/FDAnews/falseclaimsactliability/prweb13708135.htm
For more information, please visit
http://www.prweb.com/releases/FDAnews/fa[...]actliability/prweb13708135.htm
