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Results for tag: "CGMP"

Effective Annual U.S. FDA CGMP Training - Product Thumbnail Image

Effective Annual U.S. FDA CGMP Training

  • Training
  • 60 Minutes
  • United States
Creating FDA-compliant cGMP Training Program - Product Thumbnail Image

Creating FDA-compliant cGMP Training Program

  • Training
  • 60 Minutes
  • Global
Overview of Quality by Design - Product Thumbnail Image

Overview of Quality by Design

  • Training
  • Global
Bringing FDA Pharmaceutical GMPs into the 21st Century - Product Thumbnail Image

Bringing FDA Pharmaceutical GMPs into the 21st Century

  • Training
  • 60 Minutes
  • Global
Medical Device Process Validation Training for Professionals - Product Thumbnail Image

Medical Device Process Validation Training for Professionals

  • Training
  • 90 Minutes
  • Global
Implementing a Robust and Compliant Change Control Program - Product Thumbnail Image

Implementing a Robust and Compliant Change Control Program

  • Training
  • 90 Minutes
  • Global
Good Laboratory Practice Regulations - Product Thumbnail Image

Good Laboratory Practice Regulations

  • Training
  • 75 Minutes
  • Global
CGMP controlled Raw Materials - Product Thumbnail Image

CGMP controlled Raw Materials

  • Training
  • 90 Minutes
  • Global
Validation Master Plan - The Unwritten Requirements - Product Thumbnail Image

Validation Master Plan - The Unwritten Requirements

  • Training
  • 60 Minutes
  • Global
US FDA Medical Device QSR, 21 CFR 820 and Quality Management System - Product Thumbnail Image

US FDA Medical Device QSR, 21 CFR 820 and Quality Management System

  • Training
  • 90 Minutes
  • United States
Streamlining your QMS and Audit System for Remote Audits - Product Thumbnail Image

Streamlining your QMS and Audit System for Remote Audits

  • Training
  • 60 Minutes
  • Global
Good Documentation Practices (GDP) for Life Sciences - E-Learning Course - Product Thumbnail Image

Good Documentation Practices (GDP) for Life Sciences - E-Learning Course

  • Training
  • 2 Hours
  • Global
3-Hour Virtual Seminar on Master Validation Plan - The Unwritten Requirements - Webinar (Recorded) - Product Thumbnail Image

3-Hour Virtual Seminar on Master Validation Plan - The Unwritten Requirements - Webinar (Recorded)

  • Webinar
  • May 2023
  • 180 Minutes
  • Global
From
Good Manufacturing Practices (GMP) - An Introduction - Webinar (Recorded) - Product Thumbnail Image

Good Manufacturing Practices (GMP) - An Introduction - Webinar (Recorded)

  • Webinar
  • May 2023
  • 90 Minutes
  • Global
From
4-Hour Virtual Seminar on The DHF, DMR, DHR, EU MDR Technical Documentation Similarities, Differences and The Future - Webinar (Recorded) - Product Thumbnail Image

4-Hour Virtual Seminar on The DHF, DMR, DHR, EU MDR Technical Documentation Similarities, Differences and The Future - Webinar (Recorded)

  • Webinar
  • May 2023
  • 240 Minutes
  • Europe
From
4-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

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

  • Webinar
  • June 2022
  • 240 Minutes
  • Global
From
Establishing an Effective & Pragmatic Vendor Qualification Program for cGMP Compliance in the Pharmaceutical Industry - Webinar - Product Thumbnail Image

Establishing an Effective & Pragmatic Vendor Qualification Program for cGMP Compliance in the Pharmaceutical Industry - Webinar

  • Webinar
  • 90 Minutes
  • Global
From
Design History Files and Technical Files/Design Dossiers - Meeting U.S. FDA CGMPS and the EU's MDD Requirements - Product Thumbnail Image

Design History Files and Technical Files/Design Dossiers - Meeting U.S. FDA CGMPS and the EU's MDD Requirements

  • Training
  • 90 Minutes
  • Europe, United States Europe, United States
Process Validation - Overview of Why and How - Product Thumbnail Image

Process Validation - Overview of Why and How

  • Training
  • 60 Minutes
  • Global
Good Practices for Data Integrity, the new Guidance and one FDA Inspector's Experience - Product Thumbnail Image

Good Practices for Data Integrity, the new Guidance and one FDA Inspector's Experience

  • Training
  • 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