GSK to pay US$ 750 mn in settlement for operating cGMP non-compliant Cidra facility
GlaxoSmithKline has finalized a previously reported agreement in principle with the US Attorney’s Office for the District of Massachusetts and the US Department of Justice (DOJ) with respect to the investigation of the company’s former manufacturing facility in Cidra, Puerto Rico.
GSK disclosed a US$ 750 million (£500 million) charge to its second-quarter 2010 earnings on July 15 in connection with the agreement in principle. No additional charge to the company’s earnings will be recorded in connection with the settlement.
“This settlement resolves a significant and long-standing legal issue facing the company,” said PD Villarreal, GSK’s senior vice president and head of Global Litigation. "We regret that we operated the Cidra facility in a manner that was inconsistent with current Good Manufacturing Practice (cGMP) requirements and with GSK's commitment to manufacturing quality. GSK worked hard to resolve fully the manufacturing issues at the Cidra facility prior to its closure in 2009 and we are committed to continuous improvement in our manufacturing processes. Our commitment to compliance with cGMP is demonstrated by the fact that we have not received an FDA warning letter at any plant since the Cidra facility was cited in July 2002.”
This settlement resolves issues at one manufacturing facility that took place over five years ago. The plant in Cidra, Puerto Rico, was closed in 2009 due to declining demand for the medicines made there. GSK no longer owns the facility.