CDRH Ombudsman Appointed From FDA's Public Affairs Office
This article was originally published in The Gray Sheet
Executive Summary
The Center for Devices and Radiological Health's newly appointed Ombudsman and Quality Assurance Manager Les Weinstein will be responsible for revising the first draft of the device center's dispute resolution guidance, according to center Director David Feigal.
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People In Brief
CDRH needs new ombudsman: Les Weinstein served his last day as ombudsman for FDA's device center April 9 and now moves to the same post within FDA's new Center for Tobacco Products. Weinstein was appointed as CDRH's first ombudsman in 2000 to handle complaints from outside the agency and disputes between the center and companies. CDRH has yet to name a replacement (1"The Gray Sheet" March 20, 2000). Weinstein released his final annual report for the device center April 7
People In Brief
CDRH needs new ombudsman: Les Weinstein served his last day as ombudsman for FDA's device center April 9 and now moves to the same post within FDA's new Center for Tobacco Products. Weinstein was appointed as CDRH's first ombudsman in 2000 to handle complaints from outside the agency and disputes between the center and companies. CDRH has yet to name a replacement (1"The Gray Sheet" March 20, 2000). Weinstein released his final annual report for the device center April 7
ODE division directors
Dan Schulz, MD, acting director of the Division of Reproductive, Abdominal & Radiological Devices in FDA's Center for Devices and Radiological Health's Office of Device Evaluation since December 1998, is named permanent director Feb. 29. Jim Dillard, deputy director of the Division of Cardiovascular and Respiratory Devices since 1996, becomes director on March 12. Both directors will report to ODE Deputy Director Kimber Richter, MD