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Results for tag: "Pharmaceutical Regulation"

Egypt Cold Chain for Pharma & Vaccines Market - Product Thumbnail Image

Egypt Cold Chain for Pharma & Vaccines Market

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  • September 2025
  • 87 Pages
  • Egypt
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Turkey Cold Chain Infra for Pharma Market - Product Thumbnail Image

Turkey Cold Chain Infra for Pharma Market

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  • 92 Pages
  • Turkey
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Saudi Arabia Cold Chain & Pharma Logistics Market - Product Thumbnail Image

Saudi Arabia Cold Chain & Pharma Logistics Market

  • Report
  • September 2025
  • 94 Pages
  • Saudi Arabia
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UK Logistics and Cold Chain Pharma Transport Market - Product Thumbnail Image

UK Logistics and Cold Chain Pharma Transport Market

  • Report
  • September 2025
  • 90 Pages
  • United Kingdom
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France Cold Chain & Pharma Logistics Market - Product Thumbnail Image

France Cold Chain & Pharma Logistics Market

  • Report
  • September 2025
  • 98 Pages
  • France
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South America Pharmaceutical Filtration Market Outlook, 2030 - Product Thumbnail Image

South America Pharmaceutical Filtration Market Outlook, 2030

  • Report
  • May 2025
  • 83 Pages
From
Pharmaceutical Export Market in India 2024-2029 - Product Thumbnail Image

Pharmaceutical Export Market in India 2024-2029

  • Report
  • February 2025
  • 68 Pages
  • India
Writing Effective Standard Operating Procedures (SOPs) for Regulatory Compliance and Operational Excellence (Recorded) - Product Thumbnail Image

Writing Effective Standard Operating Procedures (SOPs) for Regulatory Compliance and Operational Excellence (Recorded)

  • Training
  • December 2024
  • 3 Days
  • Global
From
Drug Screening Market Size and Forecasts 2020-2030: Global and Regional Share, Trends, and Growth Opportunity Analysis by Product; Technology; Application; and End-User - Product Thumbnail Image

Drug Screening Market Size and Forecasts 2020-2030: Global and Regional Share, Trends, and Growth Opportunity Analysis by Product; Technology; Application; and End-User

  • Report
  • August 2024
  • 112 Pages
  • Global
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Terminally Sterilized Pharmaceutical Products - Parametric Release ( New USP<1222>, November 2019) and its Relationship to the new British Terminal Steriliation Methodology (March 2019) (Recorded) - Product Thumbnail Image

Terminally Sterilized Pharmaceutical Products - Parametric Release ( New USP<1222>, November 2019) and its Relationship to the new British Terminal Steriliation Methodology (March 2019) (Recorded)

  • Training
  • August 2024
  • 90 Minutes
  • United Kingdom
Good Clinical Practices (GCP) Audit and Inspection Readiness (Recorded) - Product Thumbnail Image

Good Clinical Practices (GCP) Audit and Inspection Readiness (Recorded)

  • Training
  • March 2024
  • 90 Minutes
  • Global
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eCTD Submissions - Fundamentals and Process (Recorded) - Product Thumbnail Image

eCTD Submissions - Fundamentals and Process (Recorded)

  • Training
  • February 2024
  • 60 Minutes
  • Global
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US Dietary Supplements - Regulatory Compliance Requirements, Product Claims, Labeling Issues and FDA Updates What You Must Know and Do - Webinar (Recorded) - Product Thumbnail Image

US Dietary Supplements - Regulatory Compliance Requirements, Product Claims, Labeling Issues and FDA Updates What You Must Know and Do - Webinar (Recorded)

  • Webinar
  • January 2024
  • 120 Minutes
  • United States
From
The FDA Recently Released a New Draft Guidance Related to Part 11 - Webinar (Recorded) - Product Thumbnail Image

The FDA Recently Released a New Draft Guidance Related to Part 11 - Webinar (Recorded)

  • Webinar
  • December 2023
  • 120 Minutes
  • Global
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US Drug Safety and FDA Inspection Readiness - Webinar (Recorded) - Product Thumbnail Image

US Drug Safety and FDA Inspection Readiness - Webinar (Recorded)

  • Webinar
  • December 2023
  • 180 Minutes
  • United States
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Middle East & Africa Drug Screening Market Outlook, 2028 - Product Thumbnail Image

Middle East & Africa Drug Screening Market Outlook, 2028

  • Report
  • November 2023
  • 74 Pages
  • Middle East, Africa
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3-Hour Virtual Seminar on Handling OOS Test Results and Completing Robust Investigations - Webinar (Recorded) - Product Thumbnail Image

3-Hour Virtual Seminar on Handling OOS Test Results and Completing Robust Investigations - Webinar (Recorded)

  • Webinar
  • November 2023
  • 3 Hours
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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
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3-Hour Virtual Seminar on Computer System Validation (CSV) vs. Computer Software Assurance (CSA) - Following a Waterfall vs. Agile Methodology - Webinar (Recorded) - Product Thumbnail Image

3-Hour Virtual Seminar on Computer System Validation (CSV) vs. Computer Software Assurance (CSA) - Following a Waterfall vs. Agile Methodology - Webinar (Recorded)

  • Webinar
  • October 2023
  • 3 Hours
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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
  • September 2023
  • 4 Hours
  • 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