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Results for tag: "Pharmaceutical Regulation"

6-Hour Virtual Seminar - Batch Record Review and Product Release - Webinar (Recorded) - Product Thumbnail Image

6-Hour Virtual Seminar - Batch Record Review and Product Release - Webinar (Recorded)

  • Webinar
  • November 2022
  • 360 Minutes
  • Global
From
4-Hour Virtual Seminar - Batch Record Review and Product Release - Webinar (Recorded) - Product Thumbnail Image

4-Hour Virtual Seminar - Batch Record Review and Product Release - Webinar (Recorded)

  • Webinar
  • May 2022
  • 240 Minutes
  • Global
From
6-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices, etc.) - Webinar (Recorded) - Product Thumbnail Image

6-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices, etc.) - Webinar (Recorded)

  • Webinar
  • October 2023
  • 360 Minutes
  • Global
From
How to Write SOPs for Human Error Reduction - Webinar (Recorded) - Product Thumbnail Image

How to Write SOPs for Human Error Reduction - Webinar (Recorded)

  • Webinar
  • October 2023
  • 90 Minutes
  • Global
From
6-Hour Virtual Seminar on 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA - Webinar (Recorded) - Product Thumbnail Image

6-Hour Virtual Seminar on 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA - Webinar (Recorded)

  • Webinar
  • June 2023
  • 360 Minutes
  • Global
From
How to Write SOP's for Human Error Reduction - Webinar (Recorded) - Product Thumbnail Image

How to Write SOP's for Human Error Reduction - Webinar (Recorded)

  • Webinar
  • May 2023
  • 90 Minutes
  • Global
From
Latin America Regulatory Compliance: Current Challenges in Argentina, Brazil, and Mexico - Webinar (Recorded) - Product Thumbnail Image

Latin America Regulatory Compliance: Current Challenges in Argentina, Brazil, and Mexico - Webinar (Recorded)

  • Webinar
  • May 2023
  • 90 Minutes
  • Argentina, Brazil, ... Argentina, Brazil, Mexico, Latin America
From
4-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices, etc.) - Webinar (Recorded) - Product Thumbnail Image

4-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices, etc.) - Webinar (Recorded)

  • Webinar
  • May 2022
  • 240 Minutes
  • Global
From
4-Hour Virtual Seminar on Batch Record Review and Product Release - Webinar (Recorded) - Product Thumbnail Image

4-Hour Virtual Seminar on Batch Record Review and Product Release - Webinar (Recorded)

  • Webinar
  • February 2022
  • 240 Minutes
  • Global
From
European Union Device Regulation (EU MDR) - Webinar (Recorded) - Product Thumbnail Image

European Union Device Regulation (EU MDR) - Webinar (Recorded)

  • Webinar
  • December 2021
  • 60 Minutes
  • Europe
From
Are You Ready for FDA FSMA Preventive Controls Audit? - Webinar (Recorded) - Product Thumbnail Image

Are You Ready for FDA FSMA Preventive Controls Audit? - Webinar (Recorded)

  • Webinar
  • December 2021
  • 60 Minutes
  • Global
From
FDA's Cloud Compliance & Regulations - Webinar (Recorded) - Product Thumbnail Image

FDA's Cloud Compliance & Regulations - Webinar (Recorded)

  • Webinar
  • October 2021
  • 90 Minutes
  • Global
From
Establishing an Effective & Pragmatic Vendor Qualification Program for cGMP Compliance in the Pharmaceutical Industry - Webinar - Product Thumbnail Image

Establishing an Effective & Pragmatic Vendor Qualification Program for cGMP Compliance in the Pharmaceutical Industry - Webinar

  • Webinar
  • 90 Minutes
  • Global
From
Supplier and Service Provider Controls: FDA Expectations - Product Thumbnail Image

Supplier and Service Provider Controls: FDA Expectations

  • Training
  • 120 Minutes
  • Global
How to Survive a DEA Inspection Series - For Manufacturers of Controlled Substances - Product Thumbnail Image

How to Survive a DEA Inspection Series - For Manufacturers of Controlled Substances

  • Training
  • 90 Minutes
  • Global
Avoid Documentation 'Time Bombs' - Product Thumbnail Image

Avoid Documentation 'Time Bombs'

  • Training
  • 60 Minutes
  • Global
Integrated Pharmaceutics. Applied Preformulation, Product Design, and Regulatory Science. Edition No. 2 - Product Thumbnail Image

Integrated Pharmaceutics. Applied Preformulation, Product Design, and Regulatory Science. Edition No. 2

  • Book
  • October 2022
  • 816 Pages
Toxicology and Risk Assessment. A Comprehensive Introduction. Edition No. 2 - Product Thumbnail Image

Toxicology and Risk Assessment. A Comprehensive Introduction. Edition No. 2

  • Book
  • October 2018
  • 840 Pages
The Textbook of Pharmaceutical Medicine. Edition No. 7 - Product Thumbnail Image

The Textbook of Pharmaceutical Medicine. Edition No. 7

  • Book
  • May 2013
  • 856 Pages
Nonclinical Safety Assessment. A Guide to International Pharmaceutical Regulations. Edition No. 1 - Product Thumbnail Image

Nonclinical Safety Assessment. A Guide to International Pharmaceutical Regulations. Edition No. 1

  • Book
  • April 2013
  • 488 Pages
  • Global
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The Pharmaceutical Regulation market is a sector of the pharmaceutical industry that focuses on the regulation of drugs and other related products. It is responsible for ensuring that drugs are safe and effective for use by the public. This includes the evaluation of clinical trials, the approval of new drugs, and the monitoring of drug safety and efficacy. The market also includes the enforcement of regulations and the enforcement of intellectual property rights. The Pharmaceutical Regulation market is composed of a variety of stakeholders, including pharmaceutical companies, regulatory authorities, and research institutions. Pharmaceutical companies are responsible for the development and production of drugs, while regulatory authorities are responsible for the approval and monitoring of drugs. Research institutions are responsible for conducting clinical trials and providing data to regulatory authorities. Some of the major companies in the Pharmaceutical Regulation market include Pfizer, Merck, GlaxoSmithKline, Novartis, and Johnson & Johnson. Show Less Read more