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483
•Galentic Pharma (India) Pvt. Ltd•December 8, 2022

FDA 483 - Galentic Pharma (India) Pvt. Ltd - December 08, 2022

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Record Details

An FDA inspection of Galentic Pharma (India) Pvt. Ltd, a manufacturer of sterile and non-sterile drug products, revealed significant deficiencies across its operations. The firm failed to establish and follow adequate procedures for preventing microbiological contamination in sterile products, lacked proper validation for aseptic processes, and exhibited weaknesses in its quality control unit's authority and record reconciliation. Additionally, issues were noted in laboratory controls, equipment cleaning, change control, drug product testing, employee training, stability programs, and data integrity.

Company
Galentic Pharma (India) Pvt. Ltd
Inspection Date
December 8, 2022
Product Type
Drugs
Office
Office of Biological Products Operations - Division I
People
  • Ucheabuchi C. Chudi-nwankwor
  • Sandra A. Boyd (Drug National Expert)
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ID · 8b2b2c5e-20dd-4693-8753-8827055fbc96

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