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Introduction to Effective Medical Writing

  June 09, 2009  
The Center for Professional Innovation & Education, King of Prussia, PA
October 29 & 30, 2009

Who Should Attend

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. Typical attendees include medical writers, reviewers of medical documents, clinical research managers and associates, regulatory affairs professionals, project physicians and medical monitors.

Learning Objectives

Upon completion of this course you will understand:

  • What medical writing encompasses
  • How to write documents that meet the company’s goals and objectives
  • Why publishing is an essential part of therapeutic product position
  • How to write an abstract or manuscript
  • How to control sentence structures for precise delivery of data
  • How to increase clarity and effectiveness through tone and voice
  • How create effective data displays
  • The role of the writer in producing and issuing documents
  • How to overcome Writer’s Block
  • How to produce documents within controlled timelines
  • The best ways to manage the review process
  • What kind of feedback is useful to other writers
  • How to reach concurrence in the review process
Organized by: Center for Professional Innovation & Education
Invited Speakers: info@cfpie.com
Deadline for Abstracts: n/a
Registration: http://www.cfpie.com/showitem.aspx?productid=047&source=hummolgen
E-mail: info@cfpie.com
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