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FDA Licenses for Marketing New Therapy for Rare Genetic Disease
The U.S. Food and Drug Administration today licensed for marketing the first product in the United States intended to protect people with hereditary a...

Advaxis Incorporated Provides Complete Response to FDA's Questions
Advaxis Incorporated has provided a complete response to the FDAs questions regarding the proposed use in humans of Lovaxin C, a live Listeria vaccine...

Barnett Releases Reference Guide on Form FDA 1572--Statement of Investigator
The Form FDA 1572: A Reference Guide for Clinical Researchers, Sponsors, and Monitors addresses an emerging reality in clinical research today: As the...

Integrated Medical Systems Receives FDA Clearance for World's First 'Suitcase' Intensive Care Unit
Integrated Medical Systems, a medical technology systems integrator developing fully integrated products for critical care, announced that it has rece...

Watson Receives US FDA Approval for RAPAFLO(TM) (silodosin) for the Treatment of Benign Prostatic Hyperplasia
Watson Pharmaceuticals, specialty pharmaceutical company, announced that the U.S. Food and Drug Administration (FDA) has approved RAPAFLO (silodosin)...

FDA Awards $5.2 Million in Grants to Further Food and Feed Safety
The U.S. Food and Drug Administration today announced the awarding of 17 grants to enhance food and feed safety. These grants fund major cooperative a...

FDA Detects Melamine Contamination in Flavored Drink
The U.S. Food and Drug Administration (FDA) has increased inspections and product testing efforts in response to the melamine contamination problem wh...

FDA Issues Interim Safety and Risk Assessment of Melamine and Melamine-related Compounds in Food
The U.S. Food and Drug Administration (FDA) today issued the results of its interim safety and risk assessment of melamine and melamine-related compou...

FDA Funding Will Increase in Tough Budget Year
The Alliance for a Stronger FDA today applauded Congressional actions to assure increased funding for FDA in fiscal year 2009. Under the Continuing R...

FDA Continues to Review Prasugrel New Drug Application
Daiichi Sankyo Company, confirmed that the U.S. Food and Drug Administration (FDA) did not complete its review for the prasugrel new drug application ...

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