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•Emcure Pharmaceuticals Limited•February 20, 2019

FDA 483 - Emcure Pharmaceuticals Limited - February 20, 2019

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Record Details

Emcure Pharmaceuticals Limited in Hinjwadi, India, was cited with six observations during an FDA inspection for manufacturing sterile and non-sterile drug products. The inspection revealed significant deficiencies in quality control, aseptic processing, environmental monitoring, laboratory procedures, and record-keeping, indicating a lack of thoroughness in investigations and adherence to established protocols. These issues collectively suggest a compromised state of control over sterile manufacturing operations and data integrity.

Company
Emcure Pharmaceuticals Limited
Inspection Date
February 20, 2019
Product Type
Drugs
Office
Office of Biological Products Operations - Division I
People
  • Walden H. Lee (Chemist/Investigator - Pharmaceutical Quality)
  • Doug Cadre
  • Jose E. Melendez (Quality System Specialist)
  • Linda F. Murphy (SVP Consulting & Operations)
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ID · 827e00cd-a343-4d28-a7f1-e66430275403

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