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The Electronic Common Technical Document (eCTD) - Building Comprehensive Functionality for Effective Implementation

  January 14, 2014  
Center for Professional Innovation & Education, Inc., Malvern, PA
Apr. 24 & 25, 2014

The guidance on marketing applications for drugs and biologics, known as the Common Technical Document (CTD), was finalized by the International Conference on Harmonization (ICH) in 2003. Today the CTD format is highly recommended for marketing applications in the United States, and is mandatory in other regions, including Canada, Japan, and Europe.

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. Since January 2008, FDA CDER has required all electronic submissions be in the eCTD format. FDA CBER requires the eCTD format for priority review and rolling submissions.

This course is designed as a review of current regulatory guidelines and how they affect strategies in the development, preparation, and successful submission of eCTDs. The foundation of the CTD’s organization, structure, and granularity are explained, along with their applicability on templates and submission-ready sections and reports. The program also explores modularity of submission components, and their applicability to lifecycle management for multi-region submissions.

Through presentations, interactive discussions, and review of real-life scenarios, the program covers the practical elements of building eCTDs, from structural and technical requirements to procedural and tactical planning that have been put into practice on successful applications. Technical elements, such as data formats, checksum function, validation criteria, and metadata requirements, are covered from an end-user perspective, with their practical implications clearly explained. In addition, participants will gain insight on assessing tools used in the preparation and completion of electronic submissions.

This course has been pre-approved by the Regulatory Affairs Professionals Society (RAPS) as eligible for 12 credits towards a participant's RAC recertification upon full completion.

Organized by: Center for Professional Innovation & Education
Invited Speakers: Contact info@cfpie.com for a list of course instructors
Deadline for Abstracts: n/a

E-mail: info@cfpie.com
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