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483
•Autolus Limited

FDA 483 - Autolus Limited

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Record Details

An FDA inspection of Autolus Limited (The Nucleus) in Stevenage, United Kingdom, a drug substance and drug product manufacturer, revealed significant deficiencies. Observations included incomplete validation of critical manufacturing processes and equipment, inadequate validation and monitoring of critical utilities, and insufficient disinfectant studies to prevent cross-contamination. These issues indicate a lack of assurance in product quality and control.

Company
Autolus Limited
Product Type
Drugs
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
People
  • Andrew E. Timmons
  • Jessica Chery
  • Kula N. Jha
  • Kathleen R. Jones (investigator)
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ID · d733f917-4ba8-442c-b520-200b3a56c95e

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