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Results for tag: "Out Of Specification Results"

Effective Deviation Investigators Under GMP - Product Thumbnail Image

Effective Deviation Investigators Under GMP

  • Training
  • 120 Minutes
  • Global
The Most Serious FDA 483s - How to Avoid Them - Product Thumbnail Image

The Most Serious FDA 483s - How to Avoid Them

  • Training
  • 90 Minutes
  • Global
Investigations of Microbial Data Deviations - Product Thumbnail Image

Investigations of Microbial Data Deviations

  • Training
  • 90 Minutes
  • Global
CGMP controlled Raw Materials - Product Thumbnail Image

CGMP controlled Raw Materials

  • Training
  • 90 Minutes
  • Global
Analytical Method Validation and Transfer - Product Thumbnail Image

Analytical Method Validation and Transfer

  • Training
  • 90 Minutes
  • Global
ICH Stability Requirements and Challenges - Product Thumbnail Image

ICH Stability Requirements and Challenges

  • Training
  • 60 Minutes
  • 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