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Results for tag: "Out Of Specification Results"

Investigation of Out-of-Specification Test Results - Webinar (Recorded) - Product Thumbnail Image

Investigation of Out-of-Specification Test Results - Webinar (Recorded)

  • Webinar
  • January 2022
  • 90 Minutes
  • Global
CGMP controlled Raw Materials - Webinar (Recorded) - Product Thumbnail Image

CGMP controlled Raw Materials - Webinar (Recorded)

  • Webinar
  • November 2021
  • 90 Minutes
  • Global
FDA Audit, Quality Assurance Practices, Responsibilities and Expectations (Recorded) - Product Thumbnail Image

FDA Audit, Quality Assurance Practices, Responsibilities and Expectations (Recorded)

  • Training
  • May 2021
  • 2 Days
  • Global
From
Analytical Method Validation, Verification and Transfer (Recorded) - Product Thumbnail Image

Analytical Method Validation, Verification and Transfer (Recorded)

  • Training
  • March 2021
  • 2 Days
  • Global
From
Quality Control Laboratory Compliance - cGMPs and GLPs (Recorded) - Product Thumbnail Image

Quality Control Laboratory Compliance - cGMPs and GLPs (Recorded)

  • Training
  • April 2020
  • 2 Days
  • Global
From
Analytical Method Validation and Transfer - Webinar (Recorded) - Product Thumbnail Image

Analytical Method Validation and Transfer - Webinar (Recorded)

  • Webinar
  • September 2019
  • 120 Minutes
  • Global
Analytical Method Validation and Transfer According to the New FDA Guidance - Webinar (Recorded) - Product Thumbnail Image

Analytical Method Validation and Transfer According to the New FDA Guidance - Webinar (Recorded)

  • Webinar
  • May 2019
  • 90 Minutes
  • Global
ICH Stability Requirements and Challenges - Webinar (Recorded) - Product Thumbnail Image

ICH Stability Requirements and Challenges - Webinar (Recorded)

  • Webinar
  • September 2018
  • 180 Minutes
  • Global
Approaching Unknown Cause Laboratory Investigations Using Lean Tools - Webinar (Recorded) - Product Thumbnail Image

Approaching Unknown Cause Laboratory Investigations Using Lean Tools - Webinar (Recorded)

  • Webinar
  • June 2018
  • 60 Minutes
  • Global
GMP Laboratory Training - Pack of 7 Courses - Product Thumbnail Image

GMP Laboratory Training - Pack of 7 Courses

  • Training
  • 12 Hours
  • Global
6-Hour Virtual Seminar - Batch Record Review and Product Release - Webinar (Recorded) - Product Thumbnail Image

6-Hour Virtual Seminar - Batch Record Review and Product Release - Webinar (Recorded)

  • Webinar
  • November 2022
  • 360 Minutes
  • Global
From
4-Hour Virtual Seminar - Batch Record Review and Product Release - Webinar (Recorded) - Product Thumbnail Image

4-Hour Virtual Seminar - Batch Record Review and Product Release - Webinar (Recorded)

  • Webinar
  • May 2022
  • 240 Minutes
  • Global
From
4-Hour Virtual Seminar on Batch Record Review and Product Release - Webinar (Recorded) - Product Thumbnail Image

4-Hour Virtual Seminar on Batch Record Review and Product Release - Webinar (Recorded)

  • Webinar
  • February 2022
  • 240 Minutes
  • Global
From
3-Hour Virtual Seminar on Handling OOS Test Results and Completing Robust Investigations - Webinar (Recorded) - Product Thumbnail Image

3-Hour Virtual Seminar on Handling OOS Test Results and Completing Robust Investigations - Webinar (Recorded)

  • Webinar
  • February 2021
  • 180 Minutes
  • Global
From
Understanding and Applying ICH Q3A and Q3B for Control of Impurities in Drug Substances and Drug Products - Webinar (Recorded) - Product Thumbnail Image

Understanding and Applying ICH Q3A and Q3B for Control of Impurities in Drug Substances and Drug Products - Webinar (Recorded)

  • Webinar
  • December 2020
  • 90 Minutes
  • Global
From
Handling OOS Test Results and Completing Robust Investigations - Webinar (Recorded) - Product Thumbnail Image

Handling OOS Test Results and Completing Robust Investigations - Webinar (Recorded)

  • Webinar
  • May 2019
  • 120 Minutes
  • Global
Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory - Webinar (Recorded) - Product Thumbnail Image

Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory - Webinar (Recorded)

  • Webinar
  • March 2019
  • 120 Minutes
  • Global
Laboratory Investigation of Out-of-Specification Results - Webinar (Recorded) - Product Thumbnail Image

Laboratory Investigation of Out-of-Specification Results - Webinar (Recorded)

  • Webinar
  • August 2018
  • 90 Minutes
  • Global
From
Handling OOS Test Results and Completing Robust Investigations - Webinar (Recorded) - Product Thumbnail Image

Handling OOS Test Results and Completing Robust Investigations - Webinar (Recorded)

  • Webinar
  • August 2018
  • 60 Minutes
  • Global
Pharmaceutical Microbiological Quality Assurance and Control. Practical Guide for Non-Sterile Manufacturing. Edition No. 1 - Product Thumbnail Image

Pharmaceutical Microbiological Quality Assurance and Control. Practical Guide for Non-Sterile Manufacturing. Edition No. 1

  • Book
  • January 2020
  • 592 Pages
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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