| Warning on Devices The FDA accused medical-device maker St. Jude Medical of violating the law by promoting and marketing its Epicor "surgical ablation" devices to treat a common heart-rhythm disorder without federal approval. online.wsj.com |
U.K. Approves Botox for Migraines Allergan said the U.K.'s drug regulator became the first in the world to approve Botox as a tool for preventing chronic migraine headaches. online.wsj.com |
Nektar Therapeutics Q2 2010 Earnings Call Transcript Nektar Therapeutics (NKTR)Q2 2010 Earnings CallJuly 28, 2010 10:00 am ETComplete Story » seekingalpha.com |
Sanofi Blood-Vessel Drug Fails Trial French drug maker Sanofi-Aventis said its experimental blood-vessel medicine NV1FGF failed to meet its target in a late stage clinical trial. online.wsj.com |
Medtox Scientific 3Q profit rises as demand grows [AP] - Medical test service company Medtox Scientific Inc. said Wednesday its profit grew 51 percent in the third quarter as testing volumes increased. us.rd.yahoo.com |