Drug Product Submission (NDS) Preparation in CTD and eCTD format
December 6, 2019 | 9:00 AM- 5:00 PM
The eCTD format has become mandatory in key markets for electronic submissions. Since January 2010, the European Medicines Agency has required all applications in the centralized procedure use the eCTD format. In the U.S., the eCTD format has become a requirement for all New Drug Applications, Biologics License Applications and Abbreviated
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