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Results for tag: "Out Of Specification Test"

Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FDA Guidance and Latest Expectations - Webinar (Recorded) - Product Thumbnail Image

Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FDA Guidance and Latest Expectations - Webinar (Recorded)

  • Webinar
  • September 2024
  • 120 Minutes
  • Global
From
Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FDA Guidance and Latest Expectations - Webinar (Recorded) - Product Thumbnail Image

Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FDA Guidance and Latest Expectations - Webinar (Recorded)

  • Webinar
  • December 2024
  • 120 Minutes
  • Global
From
Managing Microbiological Out of Specification (OOS) and Out of Trend (OOT) Results in Sterile and Non-Sterile Production FDA & ICH Expectations and Guidance (Recorded) - Product Thumbnail Image

Managing Microbiological Out of Specification (OOS) and Out of Trend (OOT) Results in Sterile and Non-Sterile Production FDA & ICH Expectations and Guidance (Recorded)

  • Training
  • July 2024
  • 90 Minutes
  • Global
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
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
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
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
GMP Laboratory Training - Pack of 7 Courses - Product Thumbnail Image

GMP Laboratory Training - Pack of 7 Courses

  • Training
  • 12 Hours
  • Global
EFFECTIVE INVESTIGATIONS What to Do When the Unexpected Happens! - Proper Investigation of Quality Events - Product Thumbnail Image

EFFECTIVE INVESTIGATIONS What to Do When the Unexpected Happens! - Proper Investigation of Quality Events

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

Laboratory Investigation Out-of-Specification Results

  • Training
  • 90 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
Auditing Analytical Laboratories for FDA Compliance - Product Thumbnail Image

Auditing Analytical Laboratories for FDA Compliance

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

Investigation of Out-of-Specification Test 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
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
Handling OOS Test Results and Completing Robust Investigations - Product Thumbnail Image

Handling OOS Test Results and Completing Robust Investigations

  • Training
  • 90 Minutes
  • Global
  • 19 Results (Page 1 of 1)
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Out of Specification (OOS) Test is a type of pharmaceutical manufacturing test used to detect and identify any non-conforming products. It is used to ensure that the product meets the required specifications and is safe for use. OOS Test is conducted by taking samples from the production line and testing them against the established standards. The results of the test are then compared to the established standards to determine if the product is compliant or not. If the product is found to be non-compliant, corrective action is taken to ensure that the product meets the required specifications. The OOS Test market is a growing industry, with many companies offering services to pharmaceutical manufacturers. These companies provide a range of services, such as testing, analysis, and consulting. Companies in the OOS Test market include Eurofins, SGS, Intertek, and Bureau Veritas. Show Less Read more