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 1. Eventura World
 2. Courses
 3. 3-Hours Virtual Seminar – Technical Writing for the Regulated Industries


3-HOURS VIRTUAL SEMINAR – TECHNICAL WRITING FOR THE REGULATED INDUSTRIES

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🎤  Joy McElroy |  📅  January 24, 2023   |  🕒  11 AM Eastern Time US

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DESCRIPTION: 

This technical writing training program will offer attendees an understanding of
how the reporting process supports products in research, development, and in the
marketplace. This virtual session will highlight the mandates for documentation
set forth by the regulators, such as the FDA, the ISO, and other governing
bodies. The program will train attendees on effectively reviewing and revising
documents and assessing your audience, in effect producing effective written
correspondence.

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Why You Should Attend: 

This course will address how to write effective correspondence and reports in
support of your company’s activities. Attendees will learn how to organize and
deliver information for the intended audience. They will also learn how to write
clear and readable documents, and how to revise and refine your own and others’
writing. The course will provide an overview of sound grammatical conventions,
address problematic areas of the English language, and afford opportunities to
address specific language issues.

Learning Objectives:

 * Understand the mandates for documentation set forth by the regulators, such
   as the Food and Drug Administration (FDA), the International Organization for
   Standardization (ISO), and other governing bodies
 * Know how the reporting process supports products in research, development,
   and the marketplace
 * Understand how documents work in tandem from initial correspondence about a
   project to an approved protocol, amendments, and final study report
 * Know how to produce effective written correspondence
 * Understand how to assess and write to the audience
 * Know how to organize and deliver information based on the message
 * Understand how to structure reports
 * Understand the innate structures of English grammar
 * Know how to create grammatically sound passages
 * Understand how the active and passive voices work and how to choose the most
   appropriate one for the type of writing you are doing
 * Have a working knowledge of punctuation marks and their role in making
   documents readable
 * Know how to review and revise documents
 * Understand your own writing patterns and know the answers to your questions
   about the English language
 * Have increased confidence in writing and revising documents

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Areas Covered in the Session :
 * Mandates for documentation set forth by the regulators, such as the Food and
   Drug Administration (FDA), the International Organization for Standardization
   (ISO), and other governing bodies
 * How the reporting process supports products in research, development, and the
   marketplace
 * How documents work in tandem from initial correspondence about a project to
   an approved protocol, amendments, and final study report
 * Assessing and writing to the audience to produce effective written
   correspondence
 * How the active and passive voices work and how to choose the most appropriate
   one for the type of writing you are doing
 * Reviewing and revising documents
 * Writing patterns and knowing the answers to your questions about the English
   language


Who Should Attend:
 * Research and Development Departments
 * Quality Assurance Departments
 * Information Technology Departments
 * Manufacturing Departments
 * Operations Departments
 * Production Departments
 * Documentation Departments
 * Anyone who wants an in-depth and comprehensive overview of the structure of
   the language and writing within the broad range of reporting that the
   industry requires







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Virtual Seminar Cleaning Technical Writing Regulation
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