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Pharmaceutical Manufacturing Market Research Reports

Tools for Human Error Reduction: Developing Metrics and KPI's (Key Performance Indicators) to Minimize Human Rrror Rates - Webinar (Recorded) - Product Thumbnail Image

Tools for Human Error Reduction: Developing Metrics and KPI's (Key Performance Indicators) to Minimize Human Rrror Rates - Webinar (Recorded)

  • Webinar
  • May 2018
  • 180 Pages
  • Global
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How to Implement the FDA SUPAC Guidance - Product Thumbnail Image

How to Implement the FDA SUPAC Guidance

  • Training
  • 60 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
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
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
New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines - Product Thumbnail Image

New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines

  • Training
  • 90 Minutes
  • Global
Performing an Effective, Robust and Compliant Sterility Failure Investigation: How to Avoid Common Mistakes - Product Thumbnail Image

Performing an Effective, Robust and Compliant Sterility Failure Investigation: How to Avoid Common Mistakes

  • Training
  • 90 Minutes
  • Global
How to Survive a DEA Inspection Series: For DEA Registered Analytical Labs and Research Facilities - Product Thumbnail Image

How to Survive a DEA Inspection Series: For DEA Registered Analytical Labs and Research Facilities

  • Training
  • 90 Minutes
  • Global
CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturers - Product Thumbnail Image

CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturers

  • Training
  • 60 Minutes
  • Europe
Best Practices in Preparation for an FDA Computer System Audit - Product Thumbnail Image

Best Practices in Preparation for an FDA Computer System Audit

  • Training
  • 90 Minutes
  • Global
System Suitability Testing (SST) for USP and FDA Compliance - Product Thumbnail Image

System Suitability Testing (SST) for USP and FDA Compliance

  • Training
  • 75 Minutes
  • Global
Pharmaceutical Compressed Air - Quality GMP Standards and Requirements - Product Thumbnail Image

Pharmaceutical Compressed Air - Quality GMP Standards and Requirements

  • Training
  • 60 Minutes
  • Global
Approaching Unknown Cause Laboratory Investigations Using Lean Tools - Product Thumbnail Image

Approaching Unknown Cause Laboratory Investigations Using Lean Tools

  • Training
  • 60 Minutes
  • Global
Webinar Series: eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada - Webinar - Product Thumbnail Image

Webinar Series: eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada - Webinar

  • Webinar
  • 12 Hours
  • Canada, United States, ... Canada, United States, Europe
Good Laboratory Practice Regulations - Product Thumbnail Image

Good Laboratory Practice Regulations

  • Training
  • 75 Minutes
  • Global
Equipment Cleaning Validation - Program Setup, Monitoring to Meet FDA Expectations - Product Thumbnail Image

Equipment Cleaning Validation - Program Setup, Monitoring to Meet FDA Expectations

  • Training
  • 60 Minutes
  • Global
Best Practices of Writing SOPs - Product Thumbnail Image

Best Practices of Writing SOPs

  • Training
  • 90 Minutes
  • Global
Pharmaceutical Water System: Design, Testing and Data Management - Product Thumbnail Image

Pharmaceutical Water System: Design, Testing and Data Management

  • Training
  • 90 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
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The Pharmaceutical Manufacturing market is composed of companies that produce drugs and other pharmaceutical products. These products are used to treat and prevent diseases, as well as to improve the quality of life. Pharmaceutical manufacturers are responsible for the research, development, production, and distribution of these products. They must adhere to strict regulations and standards to ensure the safety and efficacy of their products. The Pharmaceutical Manufacturing market is highly competitive, with many large companies vying for market share. Some of the major players in the market include Pfizer, Merck, Johnson & Johnson, Novartis, and GlaxoSmithKline. These companies are involved in the research, development, production, and distribution of pharmaceutical products. They are also involved in the marketing and promotion of their products. Show Less Read more