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The FDA hit RAM Pharma, a drug compounding and outsourcing firm, for numerous failures at its Idaho Falls facility, including repeat findings of microbial growth and lax air sampling. Read More
A drugmaker in the Czech Republic was listed on the EudraGMDP inspection database for serious deficiencies at its Prague facility including the presence of mold and dead insects. Read More
Acharya failed to qualify or properly monitor its raw material storage area, posing a risk for the starting material metronidazole, Swissmedic said. Read More
The FDA served Alkermes with a warning letter for serious violations in the promotion of its opioid addiction treatment Vivitrol (naltrexone for extended-release injectable suspension). Read More