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Results for tag: "FDA Regulation"

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
4-Hour Virtual Seminar on Good Laboratory Practices (GLPs) Comparing and Contrasting GMP - Webinar (Recorded) - Product Thumbnail Image

4-Hour Virtual Seminar on Good Laboratory Practices (GLPs) Comparing and Contrasting GMP - Webinar (Recorded)

  • Webinar
  • October 2023
  • 240 Minutes
  • Global
From
Introduction to Computer System Validation (Recorded) - Product Thumbnail Image

Introduction to Computer System Validation (Recorded)

  • Training
  • March 2023
  • 3 Hours
  • Global
From
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
Good Laboratory Practices by Using The Quality Management System (QMS) - Webinar (Recorded) - Product Thumbnail Image

Good Laboratory Practices by Using The Quality Management System (QMS) - Webinar (Recorded)

  • Webinar
  • December 2022
  • 4 Hours
  • Global
21 CFR Part 11, FDA's Guidance for Electronic Records and Electronic Signatures - Webinar (Recorded) - Product Thumbnail Image

21 CFR Part 11, FDA's Guidance for Electronic Records and Electronic Signatures - Webinar (Recorded)

  • Webinar
  • March 2022
  • 90 Minutes
  • Global
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
CGMP controlled Raw Materials - Webinar (Recorded) - Product Thumbnail Image

CGMP controlled Raw Materials - Webinar (Recorded)

  • Webinar
  • November 2021
  • 90 Minutes
  • Global
FDA Inspection Essentials (Recorded) - Product Thumbnail Image

FDA Inspection Essentials (Recorded)

  • Training
  • June 2021
  • 2 Days
  • Global
From
Analytical Method Validation, Verification and Transfer (Recorded) - Product Thumbnail Image

Analytical Method Validation, Verification and Transfer (Recorded)

  • Training
  • March 2021
  • 2 Days
  • Global
From
Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing (Recorded) - Product Thumbnail Image

Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing (Recorded)

  • Training
  • August 2020
  • 2 Days
  • Global
From
Applying Computer System Validation to Mobile Applications - Webinar (Recorded) - Product Thumbnail Image

Applying Computer System Validation to Mobile Applications - Webinar (Recorded)

  • Webinar
  • November 2019
  • 1 Hour
  • Global
From
Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs) - Webinar (Recorded) - Product Thumbnail Image

Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs) - Webinar (Recorded)

  • Webinar
  • October 2019
  • 180 Minutes
  • Global
Trends in FDA Compliance for Regulated Computer Systems in the Tobacco Industry - Webinar (Recorded) - Product Thumbnail Image

Trends in FDA Compliance for Regulated Computer Systems in the Tobacco Industry - Webinar (Recorded)

  • Webinar
  • April 2019
  • 90 Minutes
  • Global
How to Implement Good Clinical Practices for Successful FDA and International Regulatory Authority Inspections - Webinar (Recorded) - Product Thumbnail Image

How to Implement Good Clinical Practices for Successful FDA and International Regulatory Authority Inspections - Webinar (Recorded)

  • Webinar
  • June 2018
  • 90 Minutes
  • Global
From
6-Hour Virtual Seminar on 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA - Webinar (Recorded) - Product Thumbnail Image

6-Hour Virtual Seminar on 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA - Webinar (Recorded)

  • Webinar
  • June 2023
  • 360 Minutes
  • Global
From
3-Hour Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries - Webinar (Recorded) - Product Thumbnail Image

3-Hour Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries - Webinar (Recorded)

  • Webinar
  • May 2023
  • 180 Minutes
  • Global
From
3-Hours Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries - Webinar (Recorded) - Product Thumbnail Image

3-Hours Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries - Webinar (Recorded)

  • Webinar
  • March 2023
  • 180 Minutes
  • Global
From
21 CFR Part 11 (Electronic Records/Signatures) Compliance for Computer Systems Regulated by FDA - Webinar (Recorded) - Product Thumbnail Image

21 CFR Part 11 (Electronic Records/Signatures) Compliance for Computer Systems Regulated by FDA - Webinar (Recorded)

  • Webinar
  • March 2023
  • 90 Minutes
  • Global
From
4-Hour Virtual Seminar on 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA - Webinar (Recorded) - Product Thumbnail Image

4-Hour Virtual Seminar on 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA - Webinar (Recorded)

  • Webinar
  • June 2022
  • 240 Minutes
  • Global
From
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The FDA Regulation market within the context of Pharmaceutical Manufacturing is a highly regulated industry. The FDA is responsible for ensuring that all drugs and medical devices are safe and effective for their intended use. The FDA also sets standards for the manufacturing of pharmaceuticals, including the quality of raw materials, the manufacturing process, and the packaging and labeling of products. Companies must adhere to these standards in order to be approved for sale in the United States. The FDA also inspects pharmaceutical manufacturing facilities to ensure that they are in compliance with the regulations. Companies must also submit reports to the FDA on the safety and effectiveness of their products. The FDA Regulation market is an important part of the pharmaceutical industry, as it ensures that products are safe and effective for consumers. Companies in this market include Pfizer, Merck, Johnson & Johnson, GlaxoSmithKline, and Novartis. Show Less Read more