What does ECDT mean in FDA
Electronic Common Technical Document (eCTD) is an international standard for the presentation of regulatory information to health authorities. It is developed and managed by the International Conference on Harmonisation (ICH), and it ensures that all regulatory submissions are organized in a consistent manner. It allows companies to submit their product information electronically, rather than on physical paper copies, making it easier to track and manage submissions.
eCDT meaning in FDA in Governmental
eCDT mostly used in an acronym FDA in Category Governmental that means Electronic Common Technical Document
Shorthand: eCDT,
Full Form: Electronic Common Technical Document
For more information of "Electronic Common Technical Document", see the section below.
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Essential Questions and Answers on Electronic Common Technical Document in "GOVERNMENTAL»FDA"
Final Words:
The Electronic Common Technical Document (eCTD) provides an internationally accepted standard for submitting regulatory documents such as clinical trial data or drug applications to health authorities in a consistent, organized manner electronically instead of manual filing or other methods of submission which makes tracking these submissions much easier and more efficient overall.