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Results for tag: "Out Of Specification Results"

Pharmaceutical Quality Management Systems Market by Solution Type (Deviation, CAPA, Audit, Risk & Compliance, Inspection, Document, Change, Training Management), Deployment Mode (Cloud, On-premise), and End User (Pharmaceutical, CDMO/CRO) - Global Forecast to 2030 - Product Thumbnail Image

Pharmaceutical Quality Management Systems Market by Solution Type (Deviation, CAPA, Audit, Risk & Compliance, Inspection, Document, Change, Training Management), Deployment Mode (Cloud, On-premise), and End User (Pharmaceutical, CDMO/CRO) - Global Forecast to 2030

  • Report
  • September 2023
  • 215 Pages
  • 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
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
Quality Control Laboratory Compliance - cGMP and GLP Training (Recorded) - Product Thumbnail Image

Quality Control Laboratory Compliance - cGMP and GLP Training (Recorded)

  • Training
  • May 2024
  • 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
Quality Control Laboratory Compliance - cGMPs and GLPs Course (November 7-8, 2024) - Product Thumbnail Image

Quality Control Laboratory Compliance - cGMPs and GLPs Course (November 7-8, 2024)

  • Training
  • November 2024
  • 2 Days
  • Global
From
Analytical Methods Validation for FDA Compliance Drugs and Biologics (July 22-23, 2024) - Product Thumbnail Image

Analytical Methods Validation for FDA Compliance Drugs and Biologics (July 22-23, 2024)

  • Training
  • July 2024
  • 2 Days
  • Global
From
Quality Control Laboratory Compliance - cGMPs and GLPs Course (June 10-11, 2024) - Product Thumbnail Image

Quality Control Laboratory Compliance - cGMPs and GLPs Course (June 10-11, 2024)

  • Training
  • June 2024
  • 2 Days
  • Global
From
GMP Compliance for Quality Control and Laboratory Operations (Recorded) - Product Thumbnail Image

GMP Compliance for Quality Control and Laboratory Operations (Recorded)

  • Training
  • March 2024
  • 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
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
  • November 2023
  • 120 Minutes
  • 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 Compliance for Quality Control and Contract Laboratories - Webinar (Recorded) - Product Thumbnail Image

GMP Compliance for Quality Control and Contract Laboratories - Webinar (Recorded)

  • Webinar
  • February 2023
  • 90 Minutes
  • Global
Analytical Method Validation, Verification and Transfer [New Course] (Recorded) - Product Thumbnail Image

Analytical Method Validation, Verification and Transfer [New Course] (Recorded)

  • Training
  • February 2023
  • 2 Days
  • Global
From
FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control - Webinar (Recorded) - Product Thumbnail Image

FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control - Webinar (Recorded)

  • Webinar
  • March 2022
  • 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