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Listings 271 - 280 of 2154:

Cyberonics asks FDA approval to reduce study size
Medical device maker Cyberonics Inc. said Wednesday it has asked the Food and Drug Administration to approve reducing the number of patients involved ...
CyDex gets FDA approval of in-house drug
CyDex Pharmaceuticals said Monday that it has achieved a company first: federal approval of a drug it developed in-house. Lenexa-based CyDex said the ...
Daiichi sets up team to solve issues with US FDA
Daiichi Sankyo, the new owner of India’s largest drugmaker Ranbaxy Laboratories, said it has ‘formed a team’ to solve the ongoing issues with the US d...
Dangerous Brain Scans Under FDA Investigation
Federal health regulators are investigating reports of dangerous radiation levels at two more California hospitals, following earlier unsafe medical s...
Dangerous drug, do-nothing FDA
Research has shown that Darvocet (and its first cousin Darvon) is no more effective than acetaminophen (Tylenol) or aspirin, and perhaps it is no more...
Data shows Glaxo drug similar to placebo-US FDA
Company data for GlaxoSmithKline (nyse: GSK - news - people ) Plc's Promacta shows the experimental platelet-boosting drug works about as well as ...
Data supports Novartis malaria drug -US FDA staff
Data show Novartis AG's combination malaria drug Coartem appears to work and causes few serious side effects, U.S. Food and Drug Administration regula...
Database Risk and Compliance Adviser:You've Got Policies - But are They Working?
In managing risk and sustaining compliance around corporate databases, a key step is defining the appropriate policies. These provide clarity and serv...
Deadline On BPA Risk Assessment Missed by FDA
The Food and Drug Administration has apparently decided to wait for more thorough science before deciding whether BPA poses a threat to consumers. FDA...
Death of a Euphemism: The End of FDA’s ‘Approvable Letter’
Approvable letter — that sounds pretty good, right? Like, basically, something is on the verge of a green light? Not if you get one from the FDA about...


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