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Schering-Plough's "49 Plan," an aggressive seven-week sales push allegedly aimed at shoring up Zetia prescriptions by offering docs meals and entertainment, came under congressional scrutiny after it was reported on by the StarLedger blog Pharmalot. The FDA made deputy commissioner Janet Woodcock permanent director of the Center for Drug Evaluation and Research following a national search to fill the slot. Woodcock, who stepped in as acting director of the center following Stephen Galson's elevation to surgeon general last fall, previously headed CDER from 1994-2005. Amgen and J&J can continue to market their anemia drugs for cancer patients but their use should be restricted due to concerns of increased risk of tumor growth and death, an FDA advisory panel ruled. Related Results Merck and Schering-Plough's statin combo hits pharmacies Vytorin study raises questions about Cholesterol's Import Drug trials under pressure WALL STREET CHOICE: SCHERING-PLOUGH SHOWS PROMISE Girard Gibbs LLP Investigates Possible Securities Laws Violations Concerning...
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