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

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.

» Governmental » FDA

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.

eCDT also stands for:

All stands for ECDT

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