FDA 2012 - Introduction to the Electronic Common Technical Document

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FDA 2012 - Introduction to the Electronic Common Technical Document

Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=702180?channel=ourglocal | Edit Freely

Category Electronic Common Technical Document; eCTD Structure; eCTD Technical Aspects; eCTD submission guidelines

Deadline: January 27, 2012 | Date: January 27, 2012

Venue/Country: Palo Alto, U.S.A

Updated: 2011-11-15 20:58:48 (GMT+9)

Call For Papers - CFP

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

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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