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ECTD 101: Overview and Impact on the Regulatory Submissions Process WEBINAR Event #10217March 30, 2010 12:001:30 PM EST 11:00 AM12:30 PM CST 10:0011:30 AM MST 9:0010:30 AM PST PRESENTER INDIVIDUAL
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Individuals or organizations involved in the pharmaceutical or biotechnology industry who are seeking comprehensive insights into the electronic common technical document (ectd) process may require an ectd 101 overview.
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Ectd 101 overview provides an introduction to electronic common technical document (eCTD) submissions.
Companies or individuals submitting regulatory documents electronically are required to file ectd 101 overview.
To fill out ectd 101 overview, one needs to provide basic information about the eCTD submission process.
The purpose of ectd 101 overview is to educate stakeholders on the eCTD submission requirements.
Information on eCTD submission guidelines and best practices must be reported on ectd 101 overview.
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