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Results for tag: "FDA Data Integrity"

6-Hour Virtual Seminar on Auditing Analytical Laboratories for FDA Compliance - Webinar (Recorded) - Product Thumbnail Image

6-Hour Virtual Seminar on Auditing Analytical Laboratories for FDA Compliance - Webinar (Recorded)

  • Webinar
  • March 2022
  • 360 Minutes
  • Global
From
Laboratory Inspection and Auditing (Recorded) - Product Thumbnail Image

Laboratory Inspection and Auditing (Recorded)

  • Training
  • March 2022
  • 1 Day
  • Global
From
4-Hour Virtual Seminar on Data Integrity: Learn to Comply with the FDA Expectations and Avoid Facing Penalties - Webinar (Recorded) - Product Thumbnail Image

4-Hour Virtual Seminar on Data Integrity: Learn to Comply with the FDA Expectations and Avoid Facing Penalties - Webinar (Recorded)

  • Webinar
  • March 2022
  • 240 Minutes
  • Global
From
6-Hour Virtual Seminar on Validation and 21 CFR Part 11 Compliance of Computer Systems - Webinar (Recorded) - Product Thumbnail Image

6-Hour Virtual Seminar on Validation and 21 CFR Part 11 Compliance of Computer Systems - Webinar (Recorded)

  • Webinar
  • January 2022
  • 6 Hours
  • Global
From
21 CFR Part 11, Data Integrity, and Computer System Validation (Recorded) - Product Thumbnail Image

21 CFR Part 11, Data Integrity, and Computer System Validation (Recorded)

  • Training
  • September 2021
  • 1 Day
  • Global
From
Computer System Validation (CSV) and Data Integrity for Clinical Trials Regulated by FDA - Webinar (Recorded) - Product Thumbnail Image

Computer System Validation (CSV) and Data Integrity for Clinical Trials Regulated by FDA - Webinar (Recorded)

  • Webinar
  • October 2019
  • 3 Hours
  • Global
From
Establishing a Robust Data Integrity Program - Webinar (Recorded) - Product Thumbnail Image

Establishing a Robust Data Integrity Program - Webinar (Recorded)

  • Webinar
  • February 2019
  • 90 Minutes
  • Global
FDA Data Integrity Training: Pack of 6 Training Courses - Product Thumbnail Image

FDA Data Integrity Training: Pack of 6 Training Courses

  • Training
  • 9 Hours
  • Global
GAMP Data Integrity 21 CFR Part 11 Training Course - Product Thumbnail Image

GAMP Data Integrity 21 CFR Part 11 Training Course

  • Training
  • 90 Minutes
  • Global
GMP Data Integrity Best Practices and Regulatory Expectations for the Pharmaceutical Industry - Product Thumbnail Image

GMP Data Integrity Best Practices and Regulatory Expectations for the Pharmaceutical Industry

  • Training
  • 90 Minutes
  • Global
FDA Compliance and Enforcement Trends focused on Data Integrity - Product Thumbnail Image

FDA Compliance and Enforcement Trends focused on Data Integrity

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

GMP Laboratory Training - Pack of 7 Courses

  • Training
  • 12 Hours
  • Global
FDA Computer System Validation Training: Pack of 6 Training Courses - Product Thumbnail Image

FDA Computer System Validation Training: Pack of 6 Training Courses

  • Training
  • 8 Hours
  • Global
Preparing for a US FDA CGMP Compliance Audit Under 21 CFR 210, 211 and 820 - Product Thumbnail Image

Preparing for a US FDA CGMP Compliance Audit Under 21 CFR 210, 211 and 820

  • Training
  • 60 Minutes
  • United States
Validation for FDA and ISO 13485 Compliance: Pack of Two Courses - Product Thumbnail Image

Validation for FDA and ISO 13485 Compliance: Pack of Two Courses

  • Training
  • Global
FDA Modernization and Restructuring of the SDLC for Computer System Validation (CSV) and Compliance - Product Thumbnail Image

FDA Modernization and Restructuring of the SDLC for Computer System Validation (CSV) and Compliance

  • Training
  • 90 Minutes
  • Global
21 CFR Part 11 and QMS Software Risk-Based Implementation - Product Thumbnail Image

21 CFR Part 11 and QMS Software Risk-Based Implementation

  • Training
  • 60 Minutes
  • Global
Computer System Validation (CSV) vs. Computer System Assurance (CSA): Aligning the Agile Methodology to the GAMP®5 "V" Model and System Development Life Cycle (SDLC) Methodology - Product Thumbnail Image

Computer System Validation (CSV) vs. Computer System Assurance (CSA): Aligning the Agile Methodology to the GAMP®5 "V" Model and System Development Life Cycle (SDLC) Methodology

  • Training
  • 120 Minutes
  • Global
How to Comply with FDA Regulations for Tobacco-Related Products: Computer System Validation, 21 CFR Part 11, & Data Integrity - Product Thumbnail Image

How to Comply with FDA Regulations for Tobacco-Related Products: Computer System Validation, 21 CFR Part 11, & Data Integrity

  • Training
  • 90 Minutes
  • Global
Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements - Product Thumbnail Image

Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements

  • Training
  • 75 Minutes
  • Global
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The FDA Data Integrity market within the context of Pharmaceutical Manufacturing is focused on the development of systems and processes that ensure the accuracy and reliability of data used in the production of pharmaceuticals. This includes the implementation of data integrity protocols, such as the use of electronic records and signatures, to ensure that data is not altered or manipulated. Additionally, the market includes the development of systems and processes to ensure that data is collected, stored, and reported accurately and securely. The FDA Data Integrity market is an important part of the pharmaceutical manufacturing industry, as it helps to ensure the safety and efficacy of the products produced. It also helps to ensure compliance with regulatory requirements and to protect the reputation of the companies involved. Some companies in the FDA Data Integrity market include MasterControl, Inc., Sparta Systems, Inc., and Validation Technologies, Inc. Show Less Read more