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Pharmaceutical Manufacturing Market Research Reports

Good Documentation Practices (GDP) - Product Thumbnail Image

Good Documentation Practices (GDP)

  • Training
  • 60 Minutes
  • Global
ICH Q10 - Moving From GMPs To A Pharmaceutical Quality System - Product Thumbnail Image

ICH Q10 - Moving From GMPs To A Pharmaceutical Quality System

  • Training
  • 90 Minutes
  • Global
14 U.S. Code of Federal Regulations Part 13 Investigative and Enforcement Procedures - Product Thumbnail Image

14 U.S. Code of Federal Regulations Part 13 Investigative and Enforcement Procedures

  • Training
  • 90 Minutes
  • United States
CLIA (Clinical Laboratory Improvement Amendments) Guidelines on Quality Control and Quality Assessment - Product Thumbnail Image

CLIA (Clinical Laboratory Improvement Amendments) Guidelines on Quality Control and Quality Assessment

  • Training
  • 60 Minutes
  • Global
Deviations: What are they? Do you need to report? - Product Thumbnail Image

Deviations: What are they? Do you need to report?

  • Training
  • 60 Minutes
  • Global
Are you prepared for a regulatory audit from FDA or any other regulatory body? - Product Thumbnail Image

Are you prepared for a regulatory audit from FDA or any other regulatory body?

  • 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
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
Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements - Product Thumbnail Image

Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements

  • Training
  • 75 Minutes
  • Global
Pharmaceutical Cleaning Validation - Product Thumbnail Image

Pharmaceutical Cleaning Validation

  • Training
  • 60 Minutes
  • Global
4-Region internal audits: Medical Device Quality System audits that cover internal regulatory compliance for FDA, Europe, Canada and Japan - Product Thumbnail Image

4-Region internal audits: Medical Device Quality System audits that cover internal regulatory compliance for FDA, Europe, Canada and Japan

  • Training
  • 60 Minutes
  • Canada, Japan, Europe Canada, Japan, Europe
Complying with 21CFR Part 11-Understanding the Role of Predicate Rules - Product Thumbnail Image

Complying with 21CFR Part 11-Understanding the Role of Predicate Rules

  • Training
  • 60 Minutes
  • Global
Overview of Quality by Design - Product Thumbnail Image

Overview of Quality by Design

  • Training
  • Global
Effective Method Transfer of Complex Bioassays - Product Thumbnail Image

Effective Method Transfer of Complex Bioassays

  • Training
  • 60 Minutes
  • Global
FDA's Revised 510(k) Process: The Medical Device Professional's Guide to Successfully Preparing 510(k) Submissions and Regulatory Compliance - Product Thumbnail Image

FDA's Revised 510(k) Process: The Medical Device Professional's Guide to Successfully Preparing 510(k) Submissions and Regulatory Compliance

  • Training
  • 70 Minutes
  • Global
Dietary Supplements and Nutraceuticals: Compliance with FDA's Current Manufacturing Requirements - Product Thumbnail Image

Dietary Supplements and Nutraceuticals: Compliance with FDA's Current Manufacturing Requirements

  • Training
  • 90 Minutes
  • Global
Personnel Practices and Microbial Control in Pharmaceutical, Biotech, and Medical Device Manufacturing - Product Thumbnail Image

Personnel Practices and Microbial Control in Pharmaceutical, Biotech, and Medical Device Manufacturing

  • Training
  • 90 Minutes
  • Global
Ethics and Scientific Misconduct in Regulated Studies - Product Thumbnail Image

Ethics and Scientific Misconduct in Regulated Studies

  • Training
  • 60 Minutes
  • Global
The U.S. FDA's New Global Engagement Initiative - Product Thumbnail Image

The U.S. FDA's New Global Engagement Initiative

  • Training
  • 90 Minutes
  • United States, Global United States, Global
Dissolution Instrument Qualification to Meet Requirements and Minimize Product OOS Dissolution Results - Product Thumbnail Image

Dissolution Instrument Qualification to Meet Requirements and Minimize Product OOS Dissolution Results

  • Training
  • 120 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