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Pharmaceutical Manufacturing Market Research Reports

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
GAMP Data Integrity 21 CFR Part 11 Training Course - Product Thumbnail Image

GAMP Data Integrity 21 CFR Part 11 Training Course

  • Training
  • 90 Minutes
  • Global
Best Documentation Practices for FDA Compliance - Product Thumbnail Image

Best Documentation Practices for FDA Compliance

  • Training
  • 60 Minutes
  • Global
Equipment Qualification Basics - Product Thumbnail Image

Equipment Qualification Basics

  • Training
  • 90 Minutes
  • Global
The Investigational Medicinal Product Dossier (IMPD): EU's CTA vs. FDA's IND - Product Thumbnail Image

The Investigational Medicinal Product Dossier (IMPD): EU's CTA vs. FDA's IND

  • Training
  • 90 Minutes
  • Europe
Submitting FDA Electronic Regulatory Filings - Drug Establishment Registrations and Drug Listings - Product Thumbnail Image

Submitting FDA Electronic Regulatory Filings - Drug Establishment Registrations and Drug Listings

  • Training
  • 60 Minutes
  • Global
Executive Exposure under Strict Liability Doctrine in FDA Enforcement - Product Thumbnail Image

Executive Exposure under Strict Liability Doctrine in FDA Enforcement

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

Validation Master Planning - The Unstated Requirements

  • Training
  • 90 Minutes
  • Global
Creating Effective SOPs for Regulatory Compliance - Product Thumbnail Image

Creating Effective SOPs for Regulatory Compliance

  • Training
  • 60 Minutes
  • Global
USP Hot Topics: What's Hot Now and How to Track Coming Changes and Influence USP - Product Thumbnail Image

USP Hot Topics: What's Hot Now and How to Track Coming Changes and Influence USP

  • Training
  • 90 Minutes
  • Global
Effective Annual U.S. FDA CGMP Training - Product Thumbnail Image

Effective Annual U.S. FDA CGMP Training

  • Training
  • 60 Minutes
  • United States
Learning Design Controls through review of FDA 483 Observations - Product Thumbnail Image

Learning Design Controls through review of FDA 483 Observations

  • Training
  • 75 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