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Results for tag: "CGMP"

Central Fill Pharmacy Automation - Market Share Analysis, Industry Trends & Statistics, Growth Forecasts 2019 - 2029 - Product Thumbnail Image

Central Fill Pharmacy Automation - Market Share Analysis, Industry Trends & Statistics, Growth Forecasts 2019 - 2029

  • Report
  • February 2024
  • 110 Pages
  • Global
From
Pharmaceutical Analytical Testing Outsourcing - Market Share Analysis, Industry Trends & Statistics, Growth Forecasts 2019 - 2029 - Product Thumbnail Image

Pharmaceutical Analytical Testing Outsourcing - Market Share Analysis, Industry Trends & Statistics, Growth Forecasts 2019 - 2029

  • Report
  • February 2024
  • 113 Pages
  • Global
From
Europe Pharmaceutical Contract Manufacturing Market - Growth, Trends, COVID-19 Impact, and Forecasts (2023-2028) - Product Thumbnail Image

Europe Pharmaceutical Contract Manufacturing Market - Growth, Trends, COVID-19 Impact, and Forecasts (2023-2028)

  • Report
  • April 2023
  • 105 Pages
  • Europe
From
Pharmaceutical Contract Manufacturing and Research Services Market - Growth, Trends, COVID-19 Impact, and Forecasts (2022 - 2027) - Product Thumbnail Image

Pharmaceutical Contract Manufacturing and Research Services Market - Growth, Trends, COVID-19 Impact, and Forecasts (2022 - 2027)

  • Report
  • August 2022
  • 111 Pages
  • Global
From
USP <61>/<62> Microbiological Enumeration and Examination of Non-Sterile Products - Understanding the Current Standards for the Revised USP and Harmonized EP Microorganisms - Product Thumbnail Image

USP <61>/<62> Microbiological Enumeration and Examination of Non-Sterile Products - Understanding the Current Standards for the Revised USP and Harmonized EP Microorganisms

  • Training
  • 90 Minutes
  • Global
Process Validation Training Course (FDA and EU Annex 15: Qualifications and Validation) (Recorded) - Product Thumbnail Image

Process Validation Training Course (FDA and EU Annex 15: Qualifications and Validation) (Recorded)

  • Training
  • January 2024
  • 2 Days
  • Global
From
Master Validation Plan - The Unwritten Requirements Course (Recorded) - Product Thumbnail Image

Master Validation Plan - The Unwritten Requirements Course (Recorded)

  • Training
  • April 2025
  • 3 Hours
  • Global
From
Master Validation Plan - The Unwritten Requirements (Recorded) - Product Thumbnail Image

Master Validation Plan - The Unwritten Requirements (Recorded)

  • Training
  • November 2024
  • 3 Hours
  • Global
From
Master Validation Plan - The Unwritten Requirements (Recorded) - Product Thumbnail Image

Master Validation Plan - The Unwritten Requirements (Recorded)

  • Training
  • July 2024
  • 3 Hours
  • 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
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
OOS and OOT Investigations Course - Best Practices, Key Components and a Comprehensive Review of the FDA Requirements (Recorded) - Product Thumbnail Image

OOS and OOT Investigations Course - Best Practices, Key Components and a Comprehensive Review of the FDA Requirements (Recorded)

  • Training
  • September 2023
  • 2 Days
  • Global
From
Enhancing Quality Oversight in Pharmaceutical Contract Manufacturing Organizations (Recorded) - Product Thumbnail Image

Enhancing Quality Oversight in Pharmaceutical Contract Manufacturing Organizations (Recorded)

  • Training
  • August 2023
  • 2 Days
  • Global
From
The DHF, DMR, DHR, EU MDR Technical Documentation Similarities, Differences and The Future (Recorded) - Product Thumbnail Image

The DHF, DMR, DHR, EU MDR Technical Documentation Similarities, Differences and The Future (Recorded)

  • Training
  • June 2023
  • 1 Hour
  • Europe
From
6-Hour Virtual Seminar on The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities - Webinar (Recorded) - Product Thumbnail Image

6-Hour Virtual Seminar on The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities - Webinar (Recorded)

  • Webinar
  • February 2023
  • 360 Minutes
  • Global
From
Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation) - Product Thumbnail Image

Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)

  • Training
  • Global
From
cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA (Recorded) - Product Thumbnail Image

cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA (Recorded)

  • Training
  • March 2025
  • 3 Hours
  • Global
From
cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA (Recorded) - Product Thumbnail Image

cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA (Recorded)

  • Training
  • November 2024
  • 1 Day
  • Global
From
The 510(k) Mod Program, Breakthrough Technologies, and STeP (Recorded) - Product Thumbnail Image

The 510(k) Mod Program, Breakthrough Technologies, and STeP (Recorded)

  • Training
  • August 2024
  • 90 Minutes
  • Global
Annual Current Good Manufacturing Practices (cGMP) Training (Recorded) - Product Thumbnail Image

Annual Current Good Manufacturing Practices (cGMP) Training (Recorded)

  • Training
  • June 2024
  • 60 Minutes
  • Global
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The CGMP market is a subset of the pharmaceutical manufacturing industry, focusing on the production of drugs and other pharmaceutical products in accordance with Current Good Manufacturing Practices (CGMP). CGMPs are a set of regulations and guidelines issued by the US Food and Drug Administration (FDA) to ensure that pharmaceutical products are safe and effective. CGMPs cover all aspects of the manufacturing process, from raw materials to finished products, and include requirements for quality control, personnel training, and record keeping. The CGMP market is highly competitive, with many large and small companies offering a variety of services. Some of the major players in the market include Pfizer, Merck, GlaxoSmithKline, Novartis, Sanofi, and Johnson & Johnson. Other companies in the market include Teva Pharmaceuticals, AstraZeneca, Bayer, and Eli Lilly. Show Less Read more