Medical Dialogues14m
Govt Reconstitutes DTAB, AIOCD Protests Exclusion from Drug Regulatory Body
The Central Government, through a notification issued by the Ministry of Health and Family Welfare has officially ...
Health Affairs20h
Fosamax Lawsuit: The Importance Of State Duties To Warn Of Drug Dangers
Fosamax further defines the obligation of drug manufacturers to present clear, unambiguous, and accurate information to the ...
FDA classifies recall of Medtronic embolization devices as 'most serious'
The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", ...
Nearly a third of FDA medical device adverse events reported late: study
Reports on medical device adverse events widely exceed FDA deadlines, according to a recent study published in the BMJ. Read ...