...A serious question has been raised over Maharashtra’s narcotics control system. According to the Centre, the state’s food and drugs administration (FDA) in 2008 made possible the supply to drug firms of three times its quota of codeine phosphate. You may also...

...biotech company. Wrong. Amgen was a decent last-generation biotech company. It's terribly managed outfit living on EPO drugs for dialysis and oncology patients. True, it has a billion dollar (actually more) drug, Neupogen, but it could be subject to generic...

...but is now stepping into the limelight as the signature illness of the wars in Iraq and Afghanistan. Currently, no drug exists to stop the brain from swelling a few hours after a blow to the head, commonly from a car crash, an accidental fall, or in Iraq,...

...lapse. This week Boston Scientific Corp. halted sales of implantable defibrillators because it hadn’t told the U.S. Food and Drug Administration of changes in its manufacturing process. Not to worry. There is no reason to fear the manufacturing changes made...

...are not safe." -- Anonymous "I and many, many others are very much against any further promotion or advertising of Food and Drug Administration-Regulated Medical Products, particularly prescription drugs. I am very much in favor of outlawing the existing practice...

...and peripheral arterial disease (PAD) can be found online at www.SIRweb.org. Abstract 208: "Single Center Experience With Drug-eluting Stents for Infrapopliteal Occlusive Disease in Patients With Critical Limb Ischemia," A.M. Fischman, S.S. Shah, E. Kim, P....

...medicine to bring innovative drugs to patients with unmet medical needs. The HGS clinical development pipeline includes novel drugs to treat lupus, hepatitis C, inhalation anthrax and cancer. The Company's primary focus is rapid progress toward the commercialization...

...applications for metastatic breast, non-small cell lung, malignant melanoma, pancreatic and gastric. The U.S. Food and Drug Administration approved ABRAXANE for Injectable Suspension (paclitaxel protein-bound particles for injectable suspension) (albumin-bound) in...

...disease-free survival in patients suffering from indolent follicular non-Hodgkin's lymphoma. BiovaxID has been granted Orphan Drug Designation by both the U.S. FDA and the European EMEA. Biovest has also developed and markets a proprietary line of automated...

...Food and Drug Administration (FDA) attempted to restrict tobacco advertising to children in 1996. However, the tobacco industry successfully countered those attempts with lawsuits that stated the FDA did not have the authority to restrict tobacco advertising...