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Writing Effective Regulatory, Medical and Technical Documents

  May 17, 2019  
CfPA-The Center for Professional Advancement, Edison, NJ or Virtually
October 21-22, 2019

Who Should Attend?
This course will benefit professionals from new hires to managers in the pharmaceutical, medical device, biologics and related health industries 
who would like to write more effective documents. It is a valuable course for 
those in: 
  • Clinical Research 
  • Product Development
  • Regulatory
  • QA/QC
  • Compliance
  • Manufacturing
  • Engineers/Scientists
  • Directors and Managers
  • New Hires

Course Description
Writing accurate, concise, and clear technical documents is critical for a company’s successful interaction with the FDA and other regulatory bodies. Effective writing is a skill that must be constantly refined to produce these quality documents. 

This practical two-day accredited course will teach you methods to evaluate your writing style and apply steps to express complex ideas more clearly and concisely. Through lectures and class exercises you will learn strategies for organizing, revising, editing, and proofing documents and correspondences. Essential elements of technical report sections will also be discussed as well as how to respond to FDA requests for information.
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
   Zeinab Schwen, President, Strategic Regulatory Consulting

Zeinab Schwen has over 38 years of experience in the pharmaceutical and medical device industries. After working for major pharmaceutical companies, she founded a successful consulting and medical communications company which has been supporting the health care industry for over 27 years. In her capacity as the President of Strategic Regulatory Consulting she has provided product development, regulatory consulting, submission assistance, and medical communications services to companies nationwide. Ms. Schwen has also taught at several Universities and has led numerous regional workshops on medical, technical, and regulatory writing.


Deadline for Abstracts: n/a
Registration: Please click here for registration information.
E-mail: Jmorbit@cfpa.com
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