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Results for tag: "Pharmaceutical Quality System"

Supplier Management for Device makers and Drugmakers: Qualification, Contracts and Audits (Recorded) - Product Thumbnail Image

Supplier Management for Device makers and Drugmakers: Qualification, Contracts and Audits (Recorded)

  • Training
  • January 2025
  • 2 Days
  • Global
From
Process Validation Guidance Requirements Course (FDA and EU Annex 15: Qualifications and Validation) (Recorded) - Product Thumbnail Image

Process Validation Guidance Requirements Course (FDA and EU Annex 15: Qualifications and Validation) (Recorded)

  • Training
  • July 2024
  • 2 Days
  • Global
From
Supplier Management for Device makers and Drugmakers: Qualification, Contracts and Audits Course (May 20-21, 2025) - Product Thumbnail Image

Supplier Management for Device makers and Drugmakers: Qualification, Contracts and Audits Course (May 20-21, 2025)

  • Training
  • May 2025
  • 2 Days
  • Global
From
Process Validation for Pharmaceutical and Biologics (Recorded) - Product Thumbnail Image

Process Validation for Pharmaceutical and Biologics (Recorded)

  • Training
  • February 2025
  • 2 Days
  • Global
From
Process Validation for Pharmaceutical and Biologics (Recorded) - Product Thumbnail Image

Process Validation for Pharmaceutical and Biologics (Recorded)

  • Training
  • October 2024
  • 2 Days
  • Global
From
Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation) - Product Thumbnail Image

Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)

  • Training
  • Global
From
Statistical Elements of Implementing ICH Quality Guidelines (Recorded) - Product Thumbnail Image

Statistical Elements of Implementing ICH Quality Guidelines (Recorded)

  • Training
  • February 2024
  • 2 Days
  • Global
From
Latest Process Validation Guidance Requirements course (FDA and EU Annex 15: Qualifications and Validation) (Recorded) - Product Thumbnail Image

Latest Process Validation Guidance Requirements course (FDA and EU Annex 15: Qualifications and Validation) (Recorded)

  • Training
  • March 2023
  • 2 Days
  • Global
From
Latest Process Validation Guidance Requirements course (FDA and EU Annex 15: Qualifications and Validation) (Recorded) - Product Thumbnail Image

Latest Process Validation Guidance Requirements course (FDA and EU Annex 15: Qualifications and Validation) (Recorded)

  • Training
  • January 2023
  • 2 Days
  • Global
From
Statistical Elements of Implementing ICH Guidelines (Recorded) - Product Thumbnail Image

Statistical Elements of Implementing ICH Guidelines (Recorded)

  • Training
  • March 2022
  • 2 Days
  • Global
From
How to Prevent cGMP Violations & Warning letters - Training for Pharma Manufacturing - Product Thumbnail Image

How to Prevent cGMP Violations & Warning letters - Training for Pharma Manufacturing

  • Training
  • 8 Hours
  • Global
Good Manufacturing Practices for Active Pharmaceutical Ingredients (APIs) - Product Thumbnail Image

Good Manufacturing Practices for Active Pharmaceutical Ingredients (APIs)

  • Training
  • 90 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
Quality by Design: Establishing a Systematic Approach to Pharmaceutical Development - Webinar (Recorded) - Product Thumbnail Image

Quality by Design: Establishing a Systematic Approach to Pharmaceutical Development - Webinar (Recorded)

  • Webinar
  • October 2021
  • 60 Minutes
  • Global
From
Pharmaceutical Quality by Design. A Practical Approach. Edition No. 1. Advances in Pharmaceutical Technology - Product Thumbnail Image

Pharmaceutical Quality by Design. A Practical Approach. Edition No. 1. Advances in Pharmaceutical Technology

  • Book
  • March 2018
  • 368 Pages
Continuous Manufacturing of Pharmaceuticals. Edition No. 1. Advances in Pharmaceutical Technology - Product Thumbnail Image

Continuous Manufacturing of Pharmaceuticals. Edition No. 1. Advances in Pharmaceutical Technology

  • Book
  • September 2017
  • 632 Pages
  • 16 Results (Page 1 of 1)
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The Pharmaceutical Quality System (PQS) is a set of processes and procedures used in the pharmaceutical manufacturing industry to ensure the quality and safety of drugs and other products. It is designed to ensure that products meet the standards set by regulatory authorities and industry standards. The PQS includes processes such as quality control, quality assurance, and risk management. Quality control involves testing and inspecting products to ensure they meet the required standards. Quality assurance involves developing and implementing processes to ensure that products are consistently produced to the required standards. Risk management involves identifying and managing potential risks associated with the production of pharmaceutical products. The PQS market is highly competitive, with many companies offering a range of products and services. Some of the major players in the market include Merck, Pfizer, GlaxoSmithKline, Novartis, and Sanofi. Show Less Read more