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Results for tag: "Regulatory Document"

Regulatory Document - Site Master File - Webinar - Product Thumbnail Image

Regulatory Document - Site Master File - Webinar

  • Webinar
  • September 2016
From
CMO Supplier Quality Agreements - What you need to know to comply with new FDA & EU GMP Guidelines for contract Drug Manufacture - Webinar - 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

  • Webinar
  • June 2020
From
CMO Supplier Quality Agreements - What you need to know to comply with new FDA & EU GMP Guidelines for contract Drug Manufacture - Webinar - 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

  • Webinar
  • June 2020
From
Electronic Submissions to the FDA - eCTD Requirements - Webinar - Product Thumbnail Image

Electronic Submissions to the FDA - eCTD Requirements - Webinar

  • Webinar
  • September 2018
From
Trial Master File (TMF): FDA Expectations from Sponsors and Sites - Webinar - Product Thumbnail Image

Trial Master File (TMF): FDA Expectations from Sponsors and Sites - Webinar

  • Webinar
  • September 2018
From
CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturers - Webinar - Product Thumbnail Image

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

  • Webinar
  • August 2018
From
CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacture Event Information - Webinar - Product Thumbnail Image

CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacture Event Information - Webinar

  • Webinar
  • April 2017
From
Quality by Design for Biopharmaceuticals. Principles and Case Studies. Wiley Series in Biotechnology and Bioengineering - Product Thumbnail Image

Quality by Design for Biopharmaceuticals. Principles and Case Studies. Wiley Series in Biotechnology and Bioengineering

  • Book
  • July 2009
  • 312 Pages
The Investigational New Drug Application (IND) to Conduct FDA-regulated Clinical Trials - E-Learning Module - Product Thumbnail Image

The Investigational New Drug Application (IND) to Conduct FDA-regulated Clinical Trials - E-Learning Module

  • Training
  • 3 Pages
  • 8 Results (Page 1 of 1)
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