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Gland Pharma Limited receives EIR from USFDA for Dundigal Facility

Gland Pharma Limited receives EIR from USFDA for Dundigal Facility
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Gland Pharma Limited - Conclusion of US FDA Inspection at Dundigal Facility, Hyderabad

Gland Pharma Limited - Conclusion of US FDA Inspection at Dundigal Facility, Hyderabad
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Gland Pharma Ltd updates on US FDA Inspection at Dundigal Facility, Hyderabad

Gland Pharma Ltd has announced about the Pre-Market Inspection covering US FDA s Quality System / Current Good Manufacturing Practice regulations for Medical Devices i.e., 21 CFR Part 820 at Dundigal Facility at Hyderabad.

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USFDA concludes inspection at Gland Pharma s Hyderabad facility

It has received the Establishment Inspection Report (EIR).

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