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Results for tag: "Out Of Specification Results"

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Efficient Batch Record Design and Review (Recorded) - Product Thumbnail Image

Efficient Batch Record Design and Review (Recorded)

  • Training
  • February 2025
  • 2 Days
  • Global
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Good Manufacturing Practices (GMP) Online Course (Recorded) - Product Thumbnail Image

Good Manufacturing Practices (GMP) Online Course (Recorded)

  • Training
  • December 2024
  • 4 Days
  • Global
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Efficient Batch Record Design and Review (Recorded) - Product Thumbnail Image

Efficient Batch Record Design and Review (Recorded)

  • Training
  • November 2024
  • 2 Days
  • Global
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GMP Training for the QC Laboratory (Recorded) - Product Thumbnail Image

GMP Training for the QC Laboratory (Recorded)

  • Training
  • October 2024
  • 2 Days
  • Global
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Out of Specification Results (OOS) is a term used in the pharmaceutical manufacturing industry to describe results that do not meet the predetermined standards of quality. OOS results can be caused by a variety of factors, including incorrect raw materials, incorrect process parameters, or incorrect testing methods. OOS results can have a significant impact on the quality of the final product, and can lead to costly delays in production. The OOS Results market is comprised of companies that provide services to help pharmaceutical manufacturers identify and address OOS results. These services include consulting, training, and software solutions to help manufacturers identify and address OOS results. Companies in this market include Parexel, IQVIA, and Charles River Laboratories. Show Less Read more