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Results for tag: "FDA Warning Letter"

FDA Inspection Essentials (Recorded) - Product Thumbnail Image

FDA Inspection Essentials (Recorded)

  • Training
  • June 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
Performing an Effective, Robust and Compliant Sterility Failure Investigation: How to Avoid Common Mistakes - Webinar (Recorded) - Product Thumbnail Image

Performing an Effective, Robust and Compliant Sterility Failure Investigation: How to Avoid Common Mistakes - Webinar (Recorded)

  • Webinar
  • September 2019
  • 120 Minutes
  • Global
Surviving an FDA Sponsor Inspection - Training for Success - Webinar (Recorded) - Product Thumbnail Image

Surviving an FDA Sponsor Inspection - Training for Success - Webinar (Recorded)

  • Webinar
  • August 2019
  • 180 Minutes
  • Global
How to prepare for and host a FDA inspection and respond to 483's - Webinar (Recorded) - Product Thumbnail Image

How to prepare for and host a FDA inspection and respond to 483's - Webinar (Recorded)

  • Webinar
  • July 2019
  • 60 Minutes
  • Global
Writing Effective SOPs for the Medical Device and Pharmaceutical Industries - Webinar (Recorded) - Product Thumbnail Image

Writing Effective SOPs for the Medical Device and Pharmaceutical Industries - Webinar (Recorded)

  • Webinar
  • May 2019
  • 60 Minutes
  • Global
Good Documentation Practice and Record Keeping Regulations (FDA & EMA) - Webinar (Recorded) - Product Thumbnail Image

Good Documentation Practice and Record Keeping Regulations (FDA & EMA) - Webinar (Recorded)

  • Webinar
  • March 2019
  • 60 Minutes
  • Global
What exactly is required for 21 CFR Part 11, SaaS/Cloud, EU GDPR - Webinar (Recorded) - Product Thumbnail Image

What exactly is required for 21 CFR Part 11, SaaS/Cloud, EU GDPR - Webinar (Recorded)

  • Webinar
  • February 2019
  • 90 Minutes
  • Europe
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
Validation Master Plan - The Unwritten Requirements - Webinar (Recorded) - Product Thumbnail Image

Validation Master Plan - The Unwritten Requirements - Webinar (Recorded)

  • Webinar
  • December 2018
  • 120 Minutes
  • Global
Data Integrity - FDA's Latest Thinking - Webinar (Recorded) - Product Thumbnail Image

Data Integrity - FDA's Latest Thinking - Webinar (Recorded)

  • Webinar
  • November 2018
  • 180 Minutes
  • Global
From
Transfer of Analytical Methods According to the USP Chapter <1224> - Webinar (Recorded) - Product Thumbnail Image

Transfer of Analytical Methods According to the USP Chapter <1224> - Webinar (Recorded)

  • Webinar
  • October 2018
  • 90 Minutes
  • Global
Learning from Recent FDA Warning Letters Related to Part 11 and Computer Validation - Webinar (Recorded) - Product Thumbnail Image

Learning from Recent FDA Warning Letters Related to Part 11 and Computer Validation - Webinar (Recorded)

  • Webinar
  • September 2018
  • 90 Minutes
  • Global
System Suitability Testing (SST) for USP and FDA Compliance - Webinar (Recorded) - Product Thumbnail Image

System Suitability Testing (SST) for USP and FDA Compliance - Webinar (Recorded)

  • Webinar
  • June 2018
  • 90 Minutes
  • Global
GMP Laboratory Training - Pack of 7 Courses - Product Thumbnail Image

GMP Laboratory Training - Pack of 7 Courses

  • Training
  • 12 Hours
  • Global
Supplier and Contract Manufacturer Management for Medical Device Manufacturers - Product Thumbnail Image

Supplier and Contract Manufacturer Management for Medical Device Manufacturers

  • Training
  • Global
From
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products - Product Thumbnail Image

Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products

  • Training
  • 1 Day
  • Global
From
6-Hour Virtual Seminar on Audit like the FDA - Webinar (Recorded) - Product Thumbnail Image

6-Hour Virtual Seminar on Audit like the FDA - Webinar (Recorded)

  • Webinar
  • August 2022
  • 360 Minutes
  • Global
From
Writing Excellent SOPs - Webinar (Recorded) - Product Thumbnail Image

Writing Excellent SOPs - Webinar (Recorded)

  • Webinar
  • May 2023
  • 90 Minutes
  • Global
From
4-Hour Virtual Seminar - Batch Record Review and Product Release - Webinar (Recorded) - Product Thumbnail Image

4-Hour Virtual Seminar - Batch Record Review and Product Release - Webinar (Recorded)

  • Webinar
  • May 2022
  • 240 Minutes
  • Global
From
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The FDA Warning Letter market within the context of Pharmaceutical Manufacturing is a market that focuses on the enforcement of regulations and standards set by the U.S. Food and Drug Administration (FDA). Companies in this market are responsible for ensuring that their products meet the FDA's requirements for safety, efficacy, and quality. Companies must also comply with the FDA's Good Manufacturing Practices (GMPs) and other regulations. Companies that fail to meet these standards may receive a warning letter from the FDA, which can result in fines, product recalls, or other penalties. Companies in this market must also be aware of the latest developments in the industry, such as new regulations or changes to existing regulations. Some companies in the FDA Warning Letter market include Pfizer, Merck, Johnson & Johnson, Novartis, and GlaxoSmithKline. Show Less Read more