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Results for tag: "GMP"

21 CFR Part 11, FDA's Guidance for Electronic Records and Electronic Signatures - Product Thumbnail Image

21 CFR Part 11, FDA's Guidance for Electronic Records and Electronic Signatures

  • Training
  • 90 Minutes
  • Global
Brazilian Regulatory System for FDA Regulated Industry: Pack of 10 Training Courses - Product Thumbnail Image

Brazilian Regulatory System for FDA Regulated Industry: Pack of 10 Training Courses

  • Training
  • 16 Hours
  • Brazil
Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs) - Product Thumbnail Image

Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs)

  • Training
  • 120 Minutes
  • Global
Auditing API Facilities: A MUST to properly prepare for an FDA Regulatory API GMP Inspection - Product Thumbnail Image

Auditing API Facilities: A MUST to properly prepare for an FDA Regulatory API GMP Inspection

  • Training
  • 60 Minutes
  • Global
Become Specialized with Advertising, Promotion, and Labeling FDA Compliance - Training Bundle - Product Thumbnail Image

Become Specialized with Advertising, Promotion, and Labeling FDA Compliance - Training Bundle

  • Training
  • 4 Hours
  • Global
The New Dietary Supplement Good Manufacturing Practices - Product Thumbnail Image

The New Dietary Supplement Good Manufacturing Practices

  • Training
  • 60 Minutes
  • Global
Understanding CFR Part 210-211 Requirements for Drug Products - Product Thumbnail Image

Understanding CFR Part 210-211 Requirements for Drug Products

  • Training
  • 90 Minutes
  • Global
NEW Guidance for Industry: CGMP for Phase I Investigational Drugs - Product Thumbnail Image

NEW Guidance for Industry: CGMP for Phase I Investigational Drugs

  • Training
  • 90 Minutes
  • Global
Pack of 3 Trending Courses on USP Standards - Product Thumbnail Image

Pack of 3 Trending Courses on USP Standards

  • Training
  • 3 Hours
  • Global
Preparing for a US FDA CGMP Compliance Audit Under 21 CFR 210, 211 and 820 - Product Thumbnail Image

Preparing for a US FDA CGMP Compliance Audit Under 21 CFR 210, 211 and 820

  • Training
  • 60 Minutes
  • United States
FDA Inspections: Understanding the Core Elements - Part I - Product Thumbnail Image

FDA Inspections: Understanding the Core Elements - Part I

  • Training
  • 120 Minutes
  • Global
FDA Modernization and Restructuring of the SDLC for Computer System Validation (CSV) and Compliance - Product Thumbnail Image

FDA Modernization and Restructuring of the SDLC for Computer System Validation (CSV) and Compliance

  • Training
  • 90 Minutes
  • Global
Computer System Validation (CSV) vs. Computer System Assurance (CSA): Aligning the Agile Methodology to the GAMP®5 "V" Model and System Development Life Cycle (SDLC) Methodology - Product Thumbnail Image

Computer System Validation (CSV) vs. Computer System Assurance (CSA): Aligning the Agile Methodology to the GAMP®5 "V" Model and System Development Life Cycle (SDLC) Methodology

  • Training
  • 120 Minutes
  • Global
Effective Deviation Investigators Under GMP - Product Thumbnail Image

Effective Deviation Investigators Under GMP

  • Training
  • 120 Minutes
  • Global
cGMP 'Pitfalls' in the QC Laboratory-Preparing the QC Laboratory and Staff for an FDA Inspection - Product Thumbnail Image

cGMP 'Pitfalls' in the QC Laboratory-Preparing the QC Laboratory and Staff for an FDA Inspection

  • Training
  • 60 Minutes
  • Global
Implementation of the USP GMP Potency Bioassay Suite - Product Thumbnail Image

Implementation of the USP GMP Potency Bioassay Suite

  • Training
  • 60 Minutes
  • Global
EFFECTIVE INVESTIGATIONS What to Do When the Unexpected Happens! - Proper Investigation of Quality Events - Product Thumbnail Image

EFFECTIVE INVESTIGATIONS What to Do When the Unexpected Happens! - Proper Investigation of Quality Events

  • Training
  • 70 Minutes
  • Global
Dietary Supplements - Regulatory Compliance Requirements, Product Claims, Labeling Issues and FDA Updates - Product Thumbnail Image

Dietary Supplements - Regulatory Compliance Requirements, Product Claims, Labeling Issues and FDA Updates

  • Training
  • 90 Minutes
  • Global
Validation Master Planning - The Unstated Requirements - Product Thumbnail Image

Validation Master Planning - The Unstated Requirements

  • Training
  • 90 Minutes
  • Global
Human Error Reduction in GMP Manufacturing - Product Thumbnail Image

Human Error Reduction in GMP Manufacturing

  • Training
  • 90 Minutes
  • Global
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Good Manufacturing Practice (GMP) is a set of regulations and guidelines that govern the production of pharmaceuticals. GMP is designed to ensure that pharmaceuticals are consistently produced and controlled according to quality standards. It is intended to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. GMP covers all aspects of production from the starting materials, premises, and equipment to the training and personal hygiene of staff. Compliance with GMP is mandatory for all manufacturers of pharmaceuticals and active pharmaceutical ingredients. The GMP market is composed of companies that provide services and products related to GMP compliance. These services and products include consulting, auditing, training, and software solutions. Companies in the GMP market include Parexel, SGS, Eurofins, and NSF International. Show Less Read more