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FDA Finds Quality Documents Stuck in a Shredder at Glenmark Facility By Zachary Brennan - Published 05 December 2017

The US Food and Drug Administration (FDA) on Tuesday released a heavily redacted Form 483 sent last month to Glenmark Pharmaceuticals' Solan, India-based manufacturing facility.

Categories: News, US, FDA, Crisis management, Drugs, Ethics, Regulatory strategy

Tags: Glenmark Pharmaceuticals, Form 483