The International Regulatory Affairs Network
Introduction to Effective Medical Writing
22.04.2010 - 23.04.2010
Ort: Berlin, Germany
This course provides an overview of how to present product information clearly and concisely for the targeted audience. Hands-on exercises reinforce the course content.
This course is valuable to those who write or review documentation in support of clinical trials and regulatory submissions. It will also benefit professionals who prepare or review articles and abstracts about therapeutic products in any phase of development for professional publication. The course is particularly helpful for those new to the discipline and wish to understand the scope of medical writing.
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http://www.cfpie.com/showitem.aspx?productid=047&source=swissbio
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