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Results for tag: "Ectd"

6-Hour Virtual Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada - Webinar (Recorded) - Product Thumbnail Image

6-Hour Virtual Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada - Webinar (Recorded)

  • Webinar
  • June 2021
  • 6 Hours
  • Canada, United States, ... Canada, United States, Europe
From
eCTD Submissions - Fundamentals and Process (Recorded) - Product Thumbnail Image

eCTD Submissions - Fundamentals and Process (Recorded)

  • Training
  • February 2024
  • 60 Minutes
  • Global
From
eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada - Webinar (Recorded) - Product Thumbnail Image

eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada - Webinar (Recorded)

  • Webinar
  • December 2019
  • 12 Hours
  • Canada, United States, ... Canada, United States, Europe
Electronic Submissions to the FDA - eCTD Requirements - Webinar (Recorded) - Product Thumbnail Image

Electronic Submissions to the FDA - eCTD Requirements - Webinar (Recorded)

  • Webinar
  • September 2018
  • 90 Minutes
  • Global
4-Hour Virtual Seminar on eCTD Submissions of IND-NDA to the US FDA, EU and Canada - Webinar (Recorded) - Product Thumbnail Image

4-Hour Virtual Seminar on eCTD Submissions of IND-NDA to the US FDA, EU and Canada - Webinar (Recorded)

  • Webinar
  • September 2019
  • 4 Hours
  • Canada, United States, ... Canada, United States, Europe
From
  • 5 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