Posted: 15 Jan 2015 01:04 PM PST By Kurt R. Karst – The news came down on Thursday that FDA’s Center for Drug Evaluation and Research Director Janet Woodcock, M.D., namedKathleen “Cook” Uhl, M.D., as the permanent director of the Office of Generic Drugs (“OGD”). Although Dr. Uhl has manned the helm at OGD since March 2013 (see here), she has only done so in an acting capacity. She was tapped as Acting Director after the departure of Gregory P. Geba, M.D., who was OGD Director for only about nine months (see here). OGD has done without a longstanding permament Director since Gary J. Buehler, RPh., left FDA in March 2010 for an industry position. Keith Webber, Ph.D., who has also since left FDA for a position in industry, filled in as Acting Director after Mr. Buehler’s departure. A copy of Dr. Woodcock’s announcment of Dr. Uhl’s permanent position follows: Dear Office of Generic Drugs Staff:During her tenure as Acting Director, Dr. Uhl has overseen dramatic change within OGD, primarily as a result of FDA’s implementation of the Generic Drug User Fee Amendments of 2012. This includes significant changes in OGD operations and personnel (see here and here) – including recent changes to the Office of Pharmaceutical Quality (see here) – as well as policy changes (not all of which have been welcomed by the generic drug industry) (see here). Dr. Uhl’s accession to permanent OGD Director signals Dr. Woodcock’s confidence in Dr. Uhl’s ability to man the OGD ship through the sometimes turbulent waters of GDUFA and generic drug approvals. To many in the generic drug inductry, Uhl’s transition from acting to permanent OGD Director was also a foregone conclusion, though the position was advertised for a short time last year on USAJobs.gov. |
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