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Results for tag: "Regulatory Document"

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Cannabis Testing Services Market by Test Type, Product Type, End User, Technology, Lab Type - Global Forecast to 2030

  • Report
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  • 183 Pages
  • Global
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  • Report
  • May 2025
  • 186 Pages
  • Global
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U.K. Biotechnology & Pharmaceutical Services Outsourcing Market Size, Share & Trends Analysis Report By Service (Consulting, Regulatory Affairs), By End-use (Pharma, Biotech), And Segment Forecasts, 2021 - 2028 - Product Thumbnail Image

U.K. Biotechnology & Pharmaceutical Services Outsourcing Market Size, Share & Trends Analysis Report By Service (Consulting, Regulatory Affairs), By End-use (Pharma, Biotech), And Segment Forecasts, 2021 - 2028

  • Report
  • November 2021
  • 100 Pages
  • United Kingdom
From
Bioavailability and Bioequivalence Studies submitted in NDAs and INDs - Product Thumbnail Image

Bioavailability and Bioequivalence Studies submitted in NDAs and INDs

  • Training
  • 90 Minutes
  • Global
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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21 CFR Part 11, Data Integrity, and Computer System Validation (Recorded) - Product Thumbnail Image

21 CFR Part 11, Data Integrity, and Computer System Validation (Recorded)

  • Training
  • September 2021
  • 1 Day
  • Global
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Interpreting FDA's New Guidance Document on Risk-based Monitoring - Product Thumbnail Image

Interpreting FDA's New Guidance Document on Risk-based Monitoring

  • Training
  • 60 Minutes
  • Global
CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturers - Product Thumbnail Image

CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturers

  • Training
  • 60 Minutes
  • Europe
CMO Supplier Quality Agreements - What you need to know to comply with new FDA & EU GMP Guidelines for Contract Drug Manufacture - Webinar (Recorded) - Product Thumbnail Image

CMO Supplier Quality Agreements - What you need to know to comply with new FDA & EU GMP Guidelines for Contract Drug Manufacture - Webinar (Recorded)

  • Webinar
  • February 2023
  • 60 Minutes
  • Europe
From
  • 9 Results (Page 1 of 1)
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The Regulatory Document market within the context of Pharmaceutical Manufacturing is a highly specialized sector that focuses on the development and maintenance of documents that are required for the approval of drugs and other pharmaceutical products. These documents include clinical trial protocols, investigator brochures, and other documents that are necessary for the approval of drugs and other pharmaceutical products. The Regulatory Document market is a highly competitive sector, with companies competing to provide the best quality documents and services to their clients. Companies in this market must have a deep understanding of the regulatory requirements and processes in order to be successful. Companies in the Regulatory Document market include Parexel, ICON, Syneos Health, PPD, and Quintiles. Show Less Read more