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483
•Novartis Pharmaceuticals Corporation•August 21, 2023

Novartis Pharmaceuticals Corporation – FDA 483, Aug 21, 2023

Record Details

An FDA inspection of Novartis Pharmaceuticals Corp. in East Hanover, NJ, revealed a failure to ensure proper monitoring of a clinical study. Specifically, investigational product was not stored at the required temperature and was dispensed to subjects, with monitoring visits failing to identify these temperature excursions. This indicates a critical lapse in clinical trial oversight and product integrity.

Company
Novartis Pharmaceuticals Corporation
Inspection date
August 21, 2023
Product type
drugs
Office
New Jersey District Office
People
  • Mayar M. Mussa
  • Tyanna N. Hadley (investigator)
View Company Profile

ID · b86a870b-4f00-4ca2-a2ea-f19029e24813

Other documents for Novartis Pharmaceuticals Corporation
  • 483 - 2018-12-14December 14, 2018
  • EIR - 2017-09-07September 7, 2017
  • EIR - 2017-03-02March 2, 2017
  • EIR - 2017-01-24January 24, 2017
  • 483 - 2017-01-24January 24, 2017

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