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Results for tag: "CFR Part 11"

Computer System Validation Training Course (Recorded) - Product Thumbnail Image

Computer System Validation Training Course (Recorded)

  • Training
  • January 2025
  • 3 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
Good Distribution Practices of Pharmaceuticals and APIs Training Course (November 17-18, 2025) - Product Thumbnail Image

Good Distribution Practices of Pharmaceuticals and APIs Training Course (November 17-18, 2025)

  • Conference
  • November 2025
  • 2 Days
  • Global
Good Distribution Practices of Pharmaceuticals and APIs Training Course (July 9-10, 2025) - Product Thumbnail Image

Good Distribution Practices of Pharmaceuticals and APIs Training Course (July 9-10, 2025)

  • Conference
  • July 2025
  • 2 Days
  • Global
FDA Compliance and Clinical Trial Computer System Validation Core Requirements, Expectations and Challenges (April 9-10, 2025) - Product Thumbnail Image

FDA Compliance and Clinical Trial Computer System Validation Core Requirements, Expectations and Challenges (April 9-10, 2025)

  • Training
  • April 2025
  • 2 Days
  • Global
From
Good Distribution Practices of Pharmaceuticals and APIs Training Course (March 17-18, 2025) - Product Thumbnail Image

Good Distribution Practices of Pharmaceuticals and APIs Training Course (March 17-18, 2025)

  • Conference
  • March 2025
  • 2 Days
  • Global
GAMP® Data Integrity 21 CFR Part 11, 2-Day Training Course (Recorded) - Product Thumbnail Image

GAMP® Data Integrity 21 CFR Part 11, 2-Day Training Course (Recorded)

  • Training
  • December 2024
  • 2 Days
  • Global
From
Computer System Validation Boot Camp® (Recorded) - Product Thumbnail Image

Computer System Validation Boot Camp® (Recorded)

  • Training
  • August 2024
  • 2 Days
  • Global
From
FDA Compliance and Clinical Trial Computer System Validation Course (Recorded) - Product Thumbnail Image

FDA Compliance and Clinical Trial Computer System Validation Course (Recorded)

  • Training
  • June 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
FDA Trends for Computer System Validation (CSV) Compliance and Enforcement (May 21, 2025) - Product Thumbnail Image

FDA Trends for Computer System Validation (CSV) Compliance and Enforcement (May 21, 2025)

  • Training
  • May 2025
  • 1 Day
  • Global
From
Introduction to Computer System Validation Course (Recorded) - Product Thumbnail Image

Introduction to Computer System Validation Course (Recorded)

  • Training
  • February 2023
  • 6 Hours
  • Global
From
Master Validation Plan - The Unwritten Requirements (Recorded) - Product Thumbnail Image

Master Validation Plan - The Unwritten Requirements (Recorded)

  • Training
  • July 2024
  • 3 Hours
  • Global
From
Computer System Validation (CSV) (Recorded) - Product Thumbnail Image

Computer System Validation (CSV) (Recorded)

  • Training
  • December 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
Computer System Validation for Cloud and COTS Applications - Live, Online Training (Recorded) - Product Thumbnail Image

Computer System Validation for Cloud and COTS Applications - Live, Online Training (Recorded)

  • Training
  • May 2023
  • 3 Days
  • Global
From
Introduction to Computer System Validation (Recorded) - Product Thumbnail Image

Introduction to Computer System Validation (Recorded)

  • Training
  • April 2023
  • 3 Hours
  • Global
From
Introduction to Computer System Validation-Live, Online Training (Recorded) - Product Thumbnail Image

Introduction to Computer System Validation-Live, Online Training (Recorded)

  • Training
  • January 2025
  • 2 Days
  • Global
From
21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries - Webinar (Recorded) - Product Thumbnail Image

21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries - Webinar (Recorded)

  • Webinar
  • December 2024
  • 3 Hours
  • Global
From
Master Validation Plan - The Unwritten Requirements (Recorded) - Product Thumbnail Image

Master Validation Plan - The Unwritten Requirements (Recorded)

  • Training
  • November 2024
  • 3 Hours
  • Global
From
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The CFR Part 11 market is a subset of the pharmaceutical manufacturing industry that focuses on the implementation of electronic records and electronic signatures (ERES). This market is driven by the need for companies to comply with the FDA's regulations for the use of ERES in the pharmaceutical industry. The CFR Part 11 market is composed of companies that provide software, hardware, and services to help pharmaceutical companies comply with the FDA's regulations. These companies provide solutions such as document management systems, audit trails, and secure data storage. Companies in the CFR Part 11 market include MasterControl, Validation Technologies, and PharmaLex. Show Less Read more