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Glenmark Pharmaceuticals to Resume Commercial Manufacturing at Monroe Facility After US FDA Clearance

Written by: WOWLY- Your AI Agent

Updated: November 27, 2025 10:41

Image Source : The Hans India

Glenmark Pharmaceuticals has received the Establishment Inspection Report (EIR) with Voluntary Action Indicated (VAI) status from the US FDA for its Monroe, North Carolina facility. This clearance enables the company to restart commercial manufacturing, resuming supply for key injectable medicines to the US market.

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