Share Your Research, Maximize Your Social Impacts
Main Menu
Searching By
PARTNERS
FDA 2012 - Introduction to the Electronic Common Technical Document
Date2012-01-27
Deadline2012-01-27
VenuePalo Alto, USA - United States 
KeywordsElectronic Common Technical Document; eCTD Structure; eCTD Technical Aspects; eCTD submission guidelines
Topics/Call fo Papers
This 3-hr virtual seminar on the Electronic Common Technical Document will help you understand the background, technical aspects, document structure, and use of the electronic Common Technical Document.
Why Should You Attend:
As standards continue to evolve, this introductory course is designed to provide life sciences professionals with a foundation in the fundamental concepts of the electronic Common Technical Document (eCTD) in order to facilitate awareness and understanding of the quickly evolving regulatory landscape.
Who Will Benefit:
This workshop is designed for professionals from life sciences companies in:
- Medical Writing
- Regulatory Affairs
- Document Management
- IT Management
- Compliance
- Submission Management
- Professionals who are new to eCTD
Why Should You Attend:
As standards continue to evolve, this introductory course is designed to provide life sciences professionals with a foundation in the fundamental concepts of the electronic Common Technical Document (eCTD) in order to facilitate awareness and understanding of the quickly evolving regulatory landscape.
Who Will Benefit:
This workshop is designed for professionals from life sciences companies in:
- Medical Writing
- Regulatory Affairs
- Document Management
- IT Management
- Compliance
- Submission Management
- Professionals who are new to eCTD
Other CFPs
- Effective Documentation for Compliance in a Regulated Environment
- South Korea: Navigating the Regulatory and Clinical Trial Environment
- Incorporate FDA's New Process Validation Principles into Company Verification and Validation Planning
- The International Conference on Cultural Diplomacy in the EU
- China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
Last modified: 2011-11-15 20:58:48