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Results for tag: "Electronic Record"

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
Pharma 4.0: A Different Way to Approach GxP Products, Systems, and Compliance with FDA (Recorded) - Product Thumbnail Image

Pharma 4.0: A Different Way to Approach GxP Products, Systems, and Compliance with FDA (Recorded)

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

Introduction to Computer System Validation (Recorded)

  • Training
  • March 2023
  • 3 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
  • March 2023
  • 3 Days
  • Global
FDA Modernization and Restructuring of the SDLC for Computer System Validation and Compliance - Webinar (Recorded) - Product Thumbnail Image

FDA Modernization and Restructuring of the SDLC for Computer System Validation and Compliance - Webinar (Recorded)

  • Webinar
  • December 2022
  • 90 Minutes
  • Global
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 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
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
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
Practical Application of 21 CFR Part 11 - Product Thumbnail Image

Practical Application of 21 CFR Part 11

  • 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
21 CFR Part 11 compliance under the Obama administration - Product Thumbnail Image

21 CFR Part 11 compliance under the Obama administration

  • Training
  • 60 Minutes
  • Global
The FDA's final Medical Device Data System (MDDS) rule and its implications for currently regulated and unregulated vendors and providers - Product Thumbnail Image

The FDA's final Medical Device Data System (MDDS) rule and its implications for currently regulated and unregulated vendors and providers

  • Training
  • 65 Minutes
  • Global
Computer System Validation and Part 11 Compliance - Product Thumbnail Image

Computer System Validation and Part 11 Compliance

  • Training
  • 60 Minutes
  • Global
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The Electronic Record (ER) market within the context of Pharmaceutical Manufacturing is a rapidly growing sector. ER systems are used to store and manage data related to the production of pharmaceuticals, such as raw materials, production processes, and finished products. ER systems provide a secure and efficient way to store and access data, as well as to track and monitor production processes. ER systems also enable companies to comply with regulatory requirements and ensure product quality. ER systems are used by pharmaceutical manufacturers to improve operational efficiency, reduce costs, and ensure compliance with regulatory requirements. ER systems also enable companies to track and monitor production processes, as well as to store and access data related to the production of pharmaceuticals. Some companies in the ER market within the context of Pharmaceutical Manufacturing include Siemens, Rockwell Automation, ABB, Emerson, and Honeywell. Show Less Read more