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Pharmaceutical Manufacturing Market Research Reports

How to Prepare for, Manage, and Follow-up to an FDA Inspection - Product Thumbnail Image

How to Prepare for, Manage, and Follow-up to an FDA Inspection

  • Training
  • 60 Minutes
  • Global
Risk Management as applied to Design Control - Product Thumbnail Image

Risk Management as applied to Design Control

  • Training
  • 60 Minutes
  • Global
Violation...Deviation: Whatever you call them, you need a process to manage them - Product Thumbnail Image

Violation...Deviation: Whatever you call them, you need a process to manage them

  • Training
  • 60 Minutes
  • Global
Investigations of Microbial Data Deviations - Product Thumbnail Image

Investigations of Microbial Data Deviations

  • Training
  • 90 Minutes
  • Global
What are best practices for creating a Risk Management File? - Product Thumbnail Image

What are best practices for creating a Risk Management File?

  • Training
  • 60 Minutes
  • Global
Preparing for Regulatory Audits - Product Thumbnail Image

Preparing for Regulatory Audits

  • Training
  • 60 Minutes
  • Global
How to perform effective supplier audits, and avoid FDA 483 - Product Thumbnail Image

How to perform effective supplier audits, and avoid FDA 483

  • Training
  • 60 Minutes
  • Global
Validation of Rapid Microbiological Methods - Product Thumbnail Image

Validation of Rapid Microbiological Methods

  • Training
  • 90 Minutes
  • Global
Qualification and Audit of Suppliers and Vendors - A Risk Based Approach - Product Thumbnail Image

Qualification and Audit of Suppliers and Vendors - A Risk Based Approach

  • Training
  • 90 Minutes
  • Global
Cleaning & Cleaning Validation; an Overview - Product Thumbnail Image

Cleaning & Cleaning Validation; an Overview

  • Training
  • 60 Minutes
  • Global
21 CFR Part 11 compliance under the Obama administration - Product Thumbnail Image

21 CFR Part 11 compliance under the Obama administration

  • Training
  • 60 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
Surprise FDA GMP inspection - how to prepare for it - Product Thumbnail Image

Surprise FDA GMP inspection - how to prepare for it

  • Training
  • 90 Minutes
  • Global
Using ICH Q9 and Recent FDA Comments as the Foundation for the Planning, Development and Execution of Risk-Based Cleaning Validation Studies - Product Thumbnail Image

Using ICH Q9 and Recent FDA Comments as the Foundation for the Planning, Development and Execution of Risk-Based Cleaning Validation Studies

  • Training
  • 90 Minutes
  • Global
Residual Solvent Analysis According to USP <467> - Understanding and implementing the new USP chapter - Product Thumbnail Image

Residual Solvent Analysis According to USP <467> - Understanding and implementing the new USP chapter

  • Training
  • 60 Minutes
  • Global
Design History Files and Technical Files under US FDA and EU MDD - Product Thumbnail Image

Design History Files and Technical Files under US FDA and EU MDD

  • Training
  • 60 Minutes
  • United States, Europe United States, Europe
Practical Process Validations - Pack of Two Courses - Product Thumbnail Image

Practical Process Validations - Pack of Two Courses

  • Training
  • 90 Minutes
  • Global
Practical Process Validation Part 2 - Qualification Steps, Process Controls and Sustainability Strategies - Product Thumbnail Image

Practical Process Validation Part 2 - Qualification Steps, Process Controls and Sustainability Strategies

  • Training
  • Global
Practical Process Validation Part 1 - Validation Planning, Prerequisites and Best Practices - Product Thumbnail Image

Practical Process Validation Part 1 - Validation Planning, Prerequisites and Best Practices

  • Training
  • 90 Minutes
  • Global
Clearing up Roles and Responsibilities in the GLPs - Product Thumbnail Image

Clearing up Roles and Responsibilities in the GLPs

  • 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