Form 483

Novartis Pharmaceuticals Corporation Form 483, 2017-01-24

FDA issued a Form 483 to Novartis Pharmaceuticals Corporation on 2017-01-24 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Novartis Pharmaceuticals Corporation · East Hanover, United States · Issued January 24, 2017

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

24 Jan 2017
21 CFR 312.50

General responsibilities of sponsors

Cited by Nina Yang, Peter R Lenahan

24 Jan 2017
21 CFR 312.56(a)

Monitoring investigations

Cited by Nina Yang, Peter R Lenahan

24 Jan 2017
21 CFR 312.56(b)

Notification of FDA of termination of investigator

Cited by Nina Yang, Peter R Lenahan

24 Jan 2017
21 CFR 312.57(c)

Record retention requirement

Cited by Nina Yang, Peter R Lenahan

Inspected site

NPNovartis Pharmaceuticals CorporationEast Hanover, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 312.50Cited across public-safe Form 483 observations1x
21 CFR 312.56(a)Cited across public-safe Form 483 observations1x
21 CFR 312.56(b)Cited across public-safe Form 483 observations1x
21 CFR 312.57(c)Cited across public-safe Form 483 observations1x

Source document

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PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 4 observations

The source PDF and every observation in full, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere