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Results for tag: "FDA Inspection"

FDA Inspection (Recorded) - Product Thumbnail Image

FDA Inspection (Recorded)

  • Training
  • February 2024
  • 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
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
Quality Control Laboratory Compliance - cGMP and GLP Training (Recorded) - Product Thumbnail Image

Quality Control Laboratory Compliance - cGMP and GLP Training (Recorded)

  • Training
  • May 2024
  • 2 Days
  • Global
From
The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers (Recorded) - Product Thumbnail Image

The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers (Recorded)

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

Annual GMP Master Class 2024 (Recorded)

  • Training
  • March 2024
  • 2 Days
  • Global
From
FDA Regulatory Compliance for Drug and Biotech Product Training Course (Recorded) - Product Thumbnail Image

FDA Regulatory Compliance for Drug and Biotech Product Training Course (Recorded)

  • Training
  • March 2024
  • 2 Days
  • Global
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
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
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
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
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
Introduction to Computer System Validation Course (Recorded) - Product Thumbnail Image

Introduction to Computer System Validation Course (Recorded)

  • Training
  • February 2023
  • 6 Hours
  • Global
From
The US FDA QMSR Transition - 21 CFR 820 and ISO 13485 (Recorded) - Product Thumbnail Image

The US FDA QMSR Transition - 21 CFR 820 and ISO 13485 (Recorded)

  • Training
  • February 2024
  • 90 Minutes
  • United States
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
  • May 2023
  • 3 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
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
Managing GMP Compliance and Phase Appropriate GMP Considerations for Virtual Companies - Product Thumbnail Image

Managing GMP Compliance and Phase Appropriate GMP Considerations for Virtual Companies

  • Training
  • 2 Days
  • Global
From
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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