ComplianceOnline

Introduction to Styles in Microsoft Word for FDA Regulated Industries

Instructor: Chris Whalley
Product ID: 700152
Training Level: Intermediate
  • Duration: 60 Min

recorded version

$249.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section

Training CD

$500.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-963-2556

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This FDA compliance training will cover the basics of using Word styles and describe the fundamentals of Word styles, including character, paragraph, list and table styles.

If you’re like most people in regulated industries, you use Microsoft Word software to create and edit policies, procedures and other compliance documents.Despite the widespread use of this software, however, the most important feature of Word continues to confuse and intimidate users... styles.

Benefits:

Since Word applies styles to everything you put in your documents, learning how to use styles properly has many benefits:

  • Save time when creating or editing documents
  • Create more consistent, professional-looking documents
  • Increase the stability and efficiency of your electronic document files
  • Improved conversion from Word to other file formats, such as PDF and HTML

Areas Covered in the seminar:

  • This class will cover the basics of using Word styles.
  • Describing the fundamentals of Word styles, including character, paragraph, list and table styles
  • Creating, applying and managing styles
  • Building better document templates using styles

What attendees will learn:

At the end of this class attendees should be able to do the following activities on their own:

  • Create your own styles
  • Apply styles to text in your documents
  • Create document templates that contain your own styles

Who Will Benefit:

  • R&D Laboratory Personnel involved in pre-clinical studies
  • Quality Control Personnel who test clinical and commercial products
  • Manufacturing and Production Personnel who make clinical and commercial products
  • Quality Assurance Personnel who review and approve GxP documentation
  • Information Technology Personnel who support GxP systems

Instructor Profile:

Chris Whalley is a content management strategist focusing on FDA-regulated industries. The founder and publisher of Doxpub, Inc. (www.doxpub.com), Chris works and consults as a technical writer, business analyst, information architect and trainer. He has written and edited more than 500 GXP documents, and he has extensive experience implementing document management systems for FDA-regulated organizations ranging in size from start-ups to major commercial manufacturers.

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