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Pharmaceutical Manufacturing Market Research Reports

Effective Training Practices for FDA Compliance - Product Thumbnail Image

Effective Training Practices for FDA Compliance

  • Training
  • 75 Minutes
  • Global
How to Transition from Paper to Electronic Records in a Regulatory Environment - Product Thumbnail Image

How to Transition from Paper to Electronic Records in a Regulatory Environment

  • Training
  • 75 Minutes
  • Global
Laboratory Investigations for Out of Specification Results - Product Thumbnail Image

Laboratory Investigations for Out of Specification Results

  • Training
  • 90 Minutes
  • Global
Does your QC lab do GMP and non-GMP activities? - Product Thumbnail Image

Does your QC lab do GMP and non-GMP activities?

  • Training
  • 60 Minutes
  • Global
Change Control Best Practices: Avoiding Unintended Consequences of Changes - Product Thumbnail Image

Change Control Best Practices: Avoiding Unintended Consequences of Changes

  • Training
  • 90 Minutes
  • Global
Design Control / Ddesign and Development Requirements / Documents Under 21 CFR 820/ ISO 13485 7.3 - Product Thumbnail Image

Design Control / Ddesign and Development Requirements / Documents Under 21 CFR 820/ ISO 13485 7.3

  • Training
  • 90 Minutes
  • Global
Deconstructing EU MDR with Principles of Lean Documents and Lean Configuration - Product Thumbnail Image

Deconstructing EU MDR with Principles of Lean Documents and Lean Configuration

  • Training
  • 120 Minutes
  • Europe
The New US FDA 21 CFR 820, Quality Management System Regulation (QMSR), Medical Device CGMPs - Product Thumbnail Image

The New US FDA 21 CFR 820, Quality Management System Regulation (QMSR), Medical Device CGMPs

  • Training
  • 90 Minutes
  • United States
Drug Labeling and Packaging: Meeting Regulatory Requirements - Product Thumbnail Image

Drug Labeling and Packaging: Meeting Regulatory Requirements

  • Training
  • 60 Minutes
  • Global
US FDA Medical Device QSR (21 CFR 820) / Quality Management System - current and proposed major changes - Product Thumbnail Image

US FDA Medical Device QSR (21 CFR 820) / Quality Management System - current and proposed major changes

  • Training
  • 90 Minutes
  • United States
Design History File (DHF) Remediation using Principles of Lean Documents and Lean Configuration - Product Thumbnail Image

Design History File (DHF) Remediation using Principles of Lean Documents and Lean Configuration

  • Training
  • 90 Minutes
  • Global
How to Comply with FDA Regulations for Tobacco-Related Products: Computer System Validation, 21 CFR Part 11, & Data Integrity - Product Thumbnail Image

How to Comply with FDA Regulations for Tobacco-Related Products: Computer System Validation, 21 CFR Part 11, & Data Integrity

  • Training
  • 90 Minutes
  • Global
Predicting Product Life Using Reliability Analysis Methods - Product Thumbnail Image

Predicting Product Life Using Reliability Analysis Methods

  • Training
  • 90 Minutes
  • Global
Good Documentation Practice (GDP) and FDA Validation Compliance for Regulated Computer Systems and Data - Product Thumbnail Image

Good Documentation Practice (GDP) and FDA Validation Compliance for Regulated Computer Systems and Data

  • Training
  • 90 Minutes
  • Global
Risk Management of Raw Materials in a GMP Environment - Product Thumbnail Image

Risk Management of Raw Materials in a GMP Environment

  • 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
The 510(k), IDE, Q-Sub, De Novo, and PMA Submission and Approval Process - Product Thumbnail Image

The 510(k), IDE, Q-Sub, De Novo, and PMA Submission and Approval Process

  • Training
  • 90 Minutes
  • Global
Impact Assessment for Change Control - Product Thumbnail Image

Impact Assessment for Change Control

  • Training
  • 60 Minutes
  • Global
Conducting Effective Mock FDA Inspections - Product Thumbnail Image

Conducting Effective Mock FDA Inspections

  • Training
  • 90 Minutes
  • Global
Normality Testing: Applications and Issues - Product Thumbnail Image

Normality Testing: Applications and Issues

  • Training
  • 90 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