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Gland Pharma Ltd updates on US FDA Inspection at Dundigal Facility, Hyderabad

Published: January 4, 2023

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.

Source: equitybulls.com

Related Topics:

Tamil NaduAndhra PradeshOffice Of Product EvaluationGland Pharma LtdRadiological HealthCompany Dundigal Facility At HyderabadGland PharmaEquality CenterDundigal FacilityPharma LimitedPre Market InspectionCurrent Good Manufacturing PracticeMedical DevicesEstablishment Inspection ReportProduct EvaluationGland Pharma Limited

USFDA concludes inspection at Gland Pharma's Hyderabad facility

Published: January 4, 2023

It has received the Establishment Inspection Report (EIR).

Source: indiainfoline.com

Related Topics:

Office Of Product EvaluationRadiological HealthGland PharmaEquality CenterGland Pharma LimitedCurrent GoodDundigal FacilityEstablishment Inspection ReportProduct Evaluation