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Results for tag: "Ectd"

eCTD Submissions - Fundamentals and Process (Recorded) - Product Thumbnail Image

eCTD Submissions - Fundamentals and Process (Recorded)

  • Training
  • February 2024
  • 60 Minutes
  • Global
From
Preparing Compliant eCTD Submissions - Product Thumbnail Image

Preparing Compliant eCTD Submissions

  • Training
  • 60 Minutes
  • Global
Webinar Series: eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada - Webinar - Product Thumbnail Image

Webinar Series: eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada - Webinar

  • Webinar
  • 12 Hours
  • Canada, United States, ... Canada, United States, Europe
  • 6 Results (Page 1 of 1)
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The eCTD (electronic Common Technical Document) market is a subset of the pharmaceutical manufacturing industry. It is a system used to submit regulatory documents to health authorities in a standardized electronic format. The eCTD format is used to submit applications for new drugs, biologics, and medical devices, as well as for post-approval changes. It is also used to submit safety reports and other documents related to the manufacturing and distribution of pharmaceuticals. The eCTD market is growing as more countries adopt the format and as pharmaceutical companies look for ways to streamline their regulatory processes. Companies in the eCTD market include Accelrys, ArisGlobal, Arxspan, BioClinica, Clinipace, eClinForce, eSubmissions, and Medidata Solutions. Show Less Read more