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Results for tag: "CFR Part 11"

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
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
Lifecycle Management of Analytical Methods and Procedures : Current Trends & Your Questions Answered (Recorded) - Product Thumbnail Image

Lifecycle Management of Analytical Methods and Procedures : Current Trends & Your Questions Answered (Recorded)

  • Training
  • August 2023
  • 2 Days
  • Global
From
Computer System Validation Training Course (Recorded) - Product Thumbnail Image

Computer System Validation Training Course (Recorded)

  • Training
  • April 2024
  • 3 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
Aseptic Processing and Validation Course (Recorded) - Product Thumbnail Image

Aseptic Processing and Validation Course (Recorded)

  • Training
  • January 2024
  • 2 Days
  • Global
From
21 CFR Part 11 Data Integrity Training for CSV, CSA, SaaS/Cloud - How to Reduce Costs for Compliance (Recorded) - Product Thumbnail Image

21 CFR Part 11 Data Integrity Training for CSV, CSA, SaaS/Cloud - How to Reduce Costs for Compliance (Recorded)

  • Training
  • January 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
  • January 2024
  • 2 Days
  • Global
From
Data Integrity by Design and Pharma 4.0: Next-Gen Techniques to Approach GxP Systems, and FDA Compliance (Recorded) - Product Thumbnail Image

Data Integrity by Design and Pharma 4.0: Next-Gen Techniques to Approach GxP Systems, and FDA Compliance (Recorded)

  • Training
  • December 2023
  • 2 Days
  • Global
From
3-Hour Virtual Seminar on Computer System Validation (CSV) vs. Computer Software Assurance (CSA) - Following a Waterfall vs. Agile Methodology - Webinar (Recorded) - Product Thumbnail Image

3-Hour Virtual Seminar on Computer System Validation (CSV) vs. Computer Software Assurance (CSA) - Following a Waterfall vs. Agile Methodology - Webinar (Recorded)

  • Webinar
  • October 2023
  • 3 Hours
  • Global
From
CSV Boot Camp - 3-Day Certification Course (Recorded) - Product Thumbnail Image

CSV Boot Camp - 3-Day Certification Course (Recorded)

  • Training
  • September 2023
  • 3 Days
  • Global
From
Computer System Validation (CSV/CSA), 21 CFR Part 11, Data Integrity/Privacy Compliance for FDA-Regulated Systems (Recorded) - Product Thumbnail Image

Computer System Validation (CSV/CSA), 21 CFR Part 11, Data Integrity/Privacy Compliance for FDA-Regulated Systems (Recorded)

  • Training
  • September 2023
  • 3 Days
  • Global
From
Supplier And Contract Manufacturer Management (Recorded) - Product Thumbnail Image

Supplier And Contract Manufacturer Management (Recorded)

  • Training
  • August 2023
  • 2 Days
  • Global
From
3-Hour Virtual Seminar on Master Validation Plan - The Unwritten Requirements - Webinar (Recorded) - Product Thumbnail Image

3-Hour Virtual Seminar on Master Validation Plan - The Unwritten Requirements - Webinar (Recorded)

  • Webinar
  • May 2023
  • 180 Minutes
  • 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
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
Medical Device Process Validation Training for Professionals - Webinar (Recorded) - Product Thumbnail Image

Medical Device Process Validation Training for Professionals - Webinar (Recorded)

  • Webinar
  • March 2023
  • 90 Minutes
  • Global
From
Risk-Based Approach to CSV, 21 CFR Part 11 and FDA Compliance - Webinar (Recorded) - Product Thumbnail Image

Risk-Based Approach to CSV, 21 CFR Part 11 and FDA Compliance - Webinar (Recorded)

  • Webinar
  • April 2022
  • 90 Minutes
  • Global
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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