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Results for tag: "Out Of Specification Results"

Analytical Method Validation, Verification and Transfer Virtual Seminar (Recorded) - Product Thumbnail Image

Analytical Method Validation, Verification and Transfer Virtual Seminar (Recorded)

  • Training
  • June 2023
  • 2 Days
  • Global
From
OOS and OOT Investigations Course - Best Practices, Key Components and a Comprehensive Review of the FDA Requirements (Recorded) - Product Thumbnail Image

OOS and OOT Investigations Course - Best Practices, Key Components and a Comprehensive Review of the FDA Requirements (Recorded)

  • Training
  • September 2023
  • 2 Days
  • Global
From
Enhancing Quality Oversight in Pharmaceutical Contract Manufacturing Organizations (Recorded) - Product Thumbnail Image

Enhancing Quality Oversight in Pharmaceutical Contract Manufacturing Organizations (Recorded)

  • Training
  • August 2023
  • 2 Days
  • Global
From
A TO Z OF Analytical Method Validation, Verification and Transfer (Recorded) - Product Thumbnail Image

A TO Z OF Analytical Method Validation, Verification and Transfer (Recorded)

  • Training
  • March 2024
  • 2 Days
  • 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
  • November 2023
  • 3 Hours
  • Global
From
Analytical Methods Validation for FDA Compliance (Recorded) - Product Thumbnail Image

Analytical Methods Validation for FDA Compliance (Recorded)

  • Training
  • November 2023
  • 2 Days
  • Global
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
  • September 2023
  • 4 Hours
  • Global
From
Basic GMP Training For Quality Control Laboratory Courses (Recorded) - Product Thumbnail Image

Basic GMP Training For Quality Control Laboratory Courses (Recorded)

  • Training
  • September 2023
  • 2 Days
  • Global
From
Efficient Batch Record Review and Product Release Training - Webinar (Recorded) - Product Thumbnail Image

Efficient Batch Record Review and Product Release Training - Webinar (Recorded)

  • Webinar
  • July 2023
  • 4 Hours
  • Global
From
Basic Good Manufacturing Practice for Quality Control Laboratory Course Online (Recorded) - Product Thumbnail Image

Basic Good Manufacturing Practice for Quality Control Laboratory Course Online (Recorded)

  • Training
  • May 2023
  • 2 Days
  • Global
From
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
Analytical Method Validation, Verification and Transfer (Recorded) - Product Thumbnail Image

Analytical Method Validation, Verification and Transfer (Recorded)

  • Training
  • March 2021
  • 2 Days
  • Global
From
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
GMP Laboratory Training - Pack of 7 Courses - Product Thumbnail Image

GMP Laboratory Training - Pack of 7 Courses

  • Training
  • 12 Hours
  • Global
Investigating Out of Specification Guidance (OOS) in the Laboratory - Product Thumbnail Image

Investigating Out of Specification Guidance (OOS) in the Laboratory

  • Training
  • 60 Minutes
  • Global
Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results - Product Thumbnail Image

Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results

  • Training
  • 120 Minutes
  • Global
Managing Failure Investigations and OOS Situations - Regulatory Requirements and Strategies for Implementation - Product Thumbnail Image

Managing Failure Investigations and OOS Situations - Regulatory Requirements and Strategies for Implementation

  • Training
  • 60 Minutes
  • Global
Laboratory Investigation Out-of-Specification Results - Product Thumbnail Image

Laboratory Investigation Out-of-Specification Results

  • Training
  • 90 Minutes
  • Global
FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control - Product Thumbnail Image

FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control

  • Training
  • 90 Minutes
  • Global
Laboratory Investigations for Out of Specification Results - Product Thumbnail Image

Laboratory Investigations for Out of Specification Results

  • Training
  • 90 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