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Results for tag: "CGMP"

The 21 Elements of a 510(k) - Product Thumbnail Image

The 21 Elements of a 510(k)

  • Training
  • 90 Minutes
  • Global
Pre-Formulation and Formulation Development of Small and Large Molecules for a Lyophilized Product - Product Thumbnail Image

Pre-Formulation and Formulation Development of Small and Large Molecules for a Lyophilized Product

  • Training
  • 90 Minutes
  • Global
Design Control / Ddesign and Development Requirements / Documents Under 21 CFR 820/ ISO 13485 7.3 - Product Thumbnail Image

Design Control / Ddesign and Development Requirements / Documents Under 21 CFR 820/ ISO 13485 7.3

  • Training
  • 90 Minutes
  • Global
The New US FDA 21 CFR 820, Quality Management System Regulation (QMSR), Medical Device CGMPs - Product Thumbnail Image

The New US FDA 21 CFR 820, Quality Management System Regulation (QMSR), Medical Device CGMPs

  • Training
  • 90 Minutes
  • United States
US FDA Medical Device QSR (21 CFR 820) / Quality Management System - current and proposed major changes - Product Thumbnail Image

US FDA Medical Device QSR (21 CFR 820) / Quality Management System - current and proposed major changes

  • Training
  • 90 Minutes
  • United States
Risk Management of Raw Materials in a GMP Environment - Product Thumbnail Image

Risk Management of Raw Materials in a GMP Environment

  • Training
  • 90 Minutes
  • Global
How to Prepare for FDA Compliance - Product Thumbnail Image

How to Prepare for FDA Compliance

  • Training
  • 60 Minutes
  • Global
PASSING A US FDA GMP INSPECTION: A-Z Guaranteeing a Pass the First Time through an FDA Inspection - Product Thumbnail Image

PASSING A US FDA GMP INSPECTION: A-Z Guaranteeing a Pass the First Time through an FDA Inspection

  • Training
  • 90 Minutes
  • United States
Preparing for a U.S. FDA Audit - Product Thumbnail Image

Preparing for a U.S. FDA Audit

  • Training
  • 60 Minutes
  • United States
FDA Compliance and Quality inspections - Product Thumbnail Image

FDA Compliance and Quality inspections

  • Training
  • 60 Minutes
  • Global
Pharmaceutical Manufacturing Process Validation - Product Thumbnail Image

Pharmaceutical Manufacturing Process Validation

  • Training
  • 60 Minutes
  • Global
Making cGMP Documentation Practical - Product Thumbnail Image

Making cGMP Documentation Practical

  • Training
  • 60 Minutes
  • Global
cGMP System Strategies for Cost effective Compliance - Product Thumbnail Image

cGMP System Strategies for Cost effective Compliance

  • Training
  • 60 Minutes
  • Global
Change Control - Implementation and Management - Product Thumbnail Image

Change Control - Implementation and Management

  • Training
  • 60 Minutes
  • Global
ICH Q10 - Moving From GMPs To A Pharmaceutical Quality System - Product Thumbnail Image

ICH Q10 - Moving From GMPs To A Pharmaceutical Quality System

  • Training
  • 90 Minutes
  • Global
Technology Transfer of a Pharmaceutical Manufacturing Process - Product Thumbnail Image

Technology Transfer of a Pharmaceutical Manufacturing Process

  • Training
  • 90 Minutes
  • Global
FDA Regulatory Actions: It's Not Just about Warning Letters - Product Thumbnail Image

FDA Regulatory Actions: It's Not Just about Warning Letters

  • Training
  • 60 Minutes
  • Global
Dietary Supplements and Nutraceuticals: Compliance with FDA's Current Manufacturing Requirements - Product Thumbnail Image

Dietary Supplements and Nutraceuticals: Compliance with FDA's Current Manufacturing Requirements

  • Training
  • 90 Minutes
  • Global
US FDA's Pre-Approval Inspection Program - Product Thumbnail Image

US FDA's Pre-Approval Inspection Program

  • Training
  • 60 Minutes
  • United States
The U.S. FDA's New Global Engagement Initiative - Product Thumbnail Image

The U.S. FDA's New Global Engagement Initiative

  • Training
  • 90 Minutes
  • United States, Global United States, 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