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Results for tag: "FDA Inspection"

Annual GMP Master Class 2024 (Recorded) - Product Thumbnail Image

Annual GMP Master Class 2024 (Recorded)

  • Training
  • March 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
GMP Master Class - Get it Right to Avoid Compliance Issues (Recorded) - Product Thumbnail Image

GMP Master Class - Get it Right to Avoid Compliance Issues (Recorded)

  • Training
  • December 2023
  • 3 Days
  • Global
From
US Drug Safety and FDA Inspection Readiness - Webinar (Recorded) - Product Thumbnail Image

US Drug Safety and FDA Inspection Readiness - Webinar (Recorded)

  • Webinar
  • December 2023
  • 180 Minutes
  • United States
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
FDA Inspections and Audit Readiness Course (Recorded) - Product Thumbnail Image

FDA Inspections and Audit Readiness Course (Recorded)

  • Training
  • November 2023
  • 2 Days
  • 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
The Quality System Regulation (cGMP, 21 CFR 210 & 211 and 820) - Webinar (Recorded) - Product Thumbnail Image

The Quality System Regulation (cGMP, 21 CFR 210 & 211 and 820) - Webinar (Recorded)

  • Webinar
  • July 2023
  • 90 Minutes
  • Global
From
Successful FDA Inspections: Essential Preparation and Management Tools - What Regulators Expect and How to Prepare (Recorded) - Product Thumbnail Image

Successful FDA Inspections: Essential Preparation and Management Tools - What Regulators Expect and How to Prepare (Recorded)

  • Training
  • June 2023
  • 2 Days
  • Global
From
FDA Regulatory Compliance for Drug and Biotech Product - Past, Present and Future (Recorded) - Product Thumbnail Image

FDA Regulatory Compliance for Drug and Biotech Product - Past, Present and Future (Recorded)

  • Training
  • May 2023
  • 2 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
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
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
Ensuring Your Site Is Ready For An Fda Inspection - Webinar (Recorded) - Product Thumbnail Image

Ensuring Your Site Is Ready For An Fda Inspection - Webinar (Recorded)

  • Webinar
  • June 2022
  • 90 Minutes
  • Global
From
How to Use Quality Systems Inspection Technique (QSIT) to Your Advantage - Webinar (Recorded) - Product Thumbnail Image

How to Use Quality Systems Inspection Technique (QSIT) to Your Advantage - Webinar (Recorded)

  • Webinar
  • March 2022
  • 60 Minutes
  • Global
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
FDA Regulatory Inspection and Audit Training: Pack of 6 Training Courses - Product Thumbnail Image

FDA Regulatory Inspection and Audit Training: Pack of 6 Training Courses

  • Training
  • 7 Hours
  • Global
How to Prepare for, Manage, and Follow-up to an FDA Inspection - Product Thumbnail Image

How to Prepare for, Manage, and Follow-up to an FDA Inspection

  • Training
  • 60 Minutes
  • Global
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The FDA Inspection market within the context of Pharmaceutical Manufacturing is a highly regulated industry. The FDA inspects pharmaceutical manufacturing facilities to ensure that they are in compliance with the regulations set forth by the agency. The inspections are conducted to ensure that the products manufactured are safe and effective for their intended use. The FDA also inspects the manufacturing process to ensure that it is in compliance with Good Manufacturing Practices (GMPs). The inspections are conducted by FDA inspectors who are trained to identify any potential risks or violations of the regulations. The FDA Inspection market is an important part of the pharmaceutical manufacturing industry, as it helps to ensure the safety and efficacy of the products being manufactured. Companies in this market include Merck, Pfizer, GlaxoSmithKline, Novartis, and Johnson & Johnson. Show Less Read more