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Results for tag: "Common Technical Document"

From
Regulatory Intelligence Report for Pharmaceuticals in the U.S. - Product Thumbnail Image

Regulatory Intelligence Report for Pharmaceuticals in the U.S.

  • Report
  • October 2022
  • 15 Pages
  • United States
From
From
New Drug Approval in the European Union - Product Thumbnail Image

New Drug Approval in the European Union

  • Book
  • June 2002
  • 356 Pages
  • Europe
  • 12 Results (Page 1 of 1)
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The Common Technical Document (CTD) is a set of documents used in the drug discovery process. It is a standardized format for the submission of regulatory information to the European Medicines Agency (EMA) and other regulatory authorities. The CTD is designed to facilitate the review process by providing a consistent format for the submission of data. It is composed of five modules, each containing specific information about the drug, its development, and its safety and efficacy. The CTD is used by pharmaceutical companies, contract research organizations, and other stakeholders in the drug discovery process. The CTD market is a growing sector of the drug discovery industry. It is a key component of the regulatory process, and its use is becoming increasingly important as the industry moves towards global harmonization of standards. The CTD market is also becoming increasingly competitive, with a number of companies offering services related to the development and submission of CTDs. Some companies in the CTD market include Parexel, Quintiles, ICON, and PPD. Show Less Read more