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Medical Writing When English Is Your Second Language

 
  January 21, 2018  
     
 


CfPIE - The Center for Professional Innovation & Education, Malvern, PA USA
August 6 & 7, 2018


Medical Writing Training

Course Description - Course runs 9:00 to 5:00 both days (Breakfast & Lunch Included)

CfPIE’s medical writing courses present a comprehensive overview of the structure of American English to give non-native writers of English the tools they need to produce clear, complete, and comprehensive documents. The medical writing training covers the structure of the language and how to control the individual components, as well as the choices writers have in delivering messages. The course also addresses specific aspects of English that are problematic for individual participants. Attendees should come prepared with specific questions they want answered during the course.

Who Should Attend

This is a course for people whose native language is other than English and who must write documents in support of therapeutic product development or regulatory submissions. Participants will learn about English within the context of the type of writing the therapeutic products industry requires.  This course is valuable for pharmaceutical, medical device, and biotech professionals in drug discovery, product development, quality assurance, clinical testing, information technology, and regulatory affairs who have some understanding of English, but wish to refine their writing skills. It is also helpful for native-born writers who want to better understand the English language and how to control it.

 
 
Organized by: Center for Professional Innovation & Education
Invited Speakers:

Kay Monroe

Kay Monroe

Specialties: Quality, Management

Kay Monroe is Acting Executive Director of Zagaya. This non-profit – specializing in Malaria – works to bring innovative technologies to the problems of global health in the developing world.

Ms. Monroe has spent over 25 years with biotechnology and pharmaceutical companies around the world; working on global project teams from Research through Phase IV and introducing Project Management Offices into several companies. She has extensive experience in product lifecycles and the creation of submission documents. In addition, she has sourced both items and processes for pharmaceuticals, biologics and devices.

Ms. Monroe has held positions as Vice President of Operations, Project Management and Quality Assurance in companies such as Lundbeck, Synarc and Genentech. She has extensive experience in the start-up environment with such companies as Cerus, Dynavax and Amyris.

Ms. Monroe received her Bachelors of Science in Animal Science from UC Davis and her MBA from Golden Gate University.

 
Deadline for Abstracts: N/A
 
Registration: https://www.cfpie.com/ProductDetails.aspx?ProductID=288
E-mail: info@cfpie.com
 
 
   
 
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