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See Latest ArticlesElectronic Safety Reporting May Soon Be Mandatory, says FDA
Pharmaceutical Technology, 09/09/09
The US Food and Drug Administration announced in an Aug. 2009 release that it would like to amend postmarket safety reporting regulations “to require that manufacturers and other facilities subject to current reporting requirements submit their reports in an electronic format.”
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Cell Therapeutics Announces FDAs Oncologic Drugs Advisory Committee to Review Pixantrone for the Treatment of Relapsed/Refractory Aggressive Non-Hodgkins Lymphoma, February 2010
Cell Therapeutics, 12/18/09
Sanofi Pasteur obtains license from Syntiron to develop & commercialize vaccine to prevent Staphylococcus infections
Sanofi-aventis, 12/17/09
Telmisartan/amlodipine: approved for high blood pressure
Formulary , 12/16/09
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