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Results for tag: "CGMP"

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions (Philadelphia, PA, United States - Recorded) - Product Thumbnail Image

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions (Philadelphia, PA, United States - Recorded)

  • Training
  • March 2023
  • 2 Days
  • Global
From
Latest Process Validation Guidance Requirements course (FDA and EU Annex 15: Qualifications and Validation) (Recorded) - Product Thumbnail Image

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

  • Training
  • March 2023
  • 2 Days
  • 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 2023
  • 1 Day
  • Global
From
Medical Device Process Validation Training for Professionals - Webinar (Recorded) - Product Thumbnail Image

Medical Device Process Validation Training for Professionals - Webinar (Recorded)

  • Webinar
  • January 2023
  • 90 Minutes
  • Global
Latest Process Validation Guidance Requirements course (FDA and EU Annex 15: Qualifications and Validation) (Recorded) - Product Thumbnail Image

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

  • Training
  • January 2023
  • 2 Days
  • Global
From
Laboratory Inspection and Auditing (Recorded) - Product Thumbnail Image

Laboratory Inspection and Auditing (Recorded)

  • Training
  • March 2022
  • 1 Day
  • Global
From
US FDA Medical Device QSR, 21 CFR 820 and Quality Management System - Webinar (Recorded) - Product Thumbnail Image

US FDA Medical Device QSR, 21 CFR 820 and Quality Management System - Webinar (Recorded)

  • Webinar
  • March 2022
  • 90 Minutes
  • United States
Building a Vendor Qualification Program for FDA Regulated Industries (Recorded) - Product Thumbnail Image

Building a Vendor Qualification Program for FDA Regulated Industries (Recorded)

  • Training
  • February 2022
  • 2 Days
  • Global
From
Implementing a Robust and Compliant Change Control Program - Webinar (Recorded) - Product Thumbnail Image

Implementing a Robust and Compliant Change Control Program - Webinar (Recorded)

  • Webinar
  • December 2021
  • 90 Minutes
  • Global
CGMP controlled Raw Materials - Webinar (Recorded) - Product Thumbnail Image

CGMP controlled Raw Materials - Webinar (Recorded)

  • Webinar
  • November 2021
  • 90 Minutes
  • Global
FDA Inspection Essentials (Recorded) - Product Thumbnail Image

FDA Inspection Essentials (Recorded)

  • Training
  • June 2021
  • 2 Days
  • Global
From
Quality Control Laboratory Compliance - cGMPs and GLPs (Recorded) - Product Thumbnail Image

Quality Control Laboratory Compliance - cGMPs and GLPs (Recorded)

  • Training
  • April 2020
  • 2 Days
  • Global
From
Aseptic Processing Overview and Validation - Webinar (Recorded) - Product Thumbnail Image

Aseptic Processing Overview and Validation - Webinar (Recorded)

  • Webinar
  • November 2019
  • 120 Minutes
  • Global
Analytical Method Validation and Transfer - Webinar (Recorded) - Product Thumbnail Image

Analytical Method Validation and Transfer - Webinar (Recorded)

  • Webinar
  • September 2019
  • 120 Minutes
  • Global
New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines - Webinar (Recorded) - Product Thumbnail Image

New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines - Webinar (Recorded)

  • Webinar
  • May 2019
  • 180 Minutes
  • Global
Supplier Quality Assurance Agreements: Why a General Supply Agreement May Not Be Enough with Some Suppliers - Webinar (Recorded) - Product Thumbnail Image

Supplier Quality Assurance Agreements: Why a General Supply Agreement May Not Be Enough with Some Suppliers - Webinar (Recorded)

  • Webinar
  • May 2019
  • 90 Minutes
  • Global
ASTM 2500: Lessons Learned Through a Decade of Implementation - Webinar (Recorded) - Product Thumbnail Image

ASTM 2500: Lessons Learned Through a Decade of Implementation - Webinar (Recorded)

  • Webinar
  • April 2019
  • 90 Minutes
  • Global
Validation Master Plan - The Unwritten Requirements - Webinar (Recorded) - Product Thumbnail Image

Validation Master Plan - The Unwritten Requirements - Webinar (Recorded)

  • Webinar
  • December 2018
  • 120 Minutes
  • Global
Data Integrity - FDA's Latest Thinking - Webinar (Recorded) - Product Thumbnail Image

Data Integrity - FDA's Latest Thinking - Webinar (Recorded)

  • Webinar
  • November 2018
  • 180 Minutes
  • Global
From
Good Manufacturing Practices (GMP) Certification Course - Product Thumbnail Image

Good Manufacturing Practices (GMP) Certification Course

  • Training
  • 17 Hours
  • Global
From
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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