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Indian drugmaker failed to notify FDA multiple times about issues with its sterile injectables: letter

Consumer complaints are a serious issues for drugmakers, particularly for those making sterile injectables. When a complaint does come in, companies are supposed to notify the FDA right away. But what happens when a drugmaker doesn’t do that—repeatedly? Despite admitting that equipment at its Telanga, India, plant was faulty and could have produced improperly sealed… Read More »