FDA Knew Drugmaker Had Poor Record. It Waited Four Years to Inspect One Factory.

The Food and Drug Administration is cracking down on a generic drugmaker that was the subject of a ProPublica investigation last year, citing problems with safety tests that delayed the recall of a medicine linked to deaths in the U.S. In December, ProPublica reported that a Glenmark Pharmaceuticals factory in central India was responsible for an outsized share of recalls for pills that didn’…

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This post has been syndicated from Truthout, where it was published under this address.