Reducing the Cost of Creating Documents for FDA-Regulated Industries

Instructor: Chris Whalley
Product ID: 700126
Training Level: Basic to Intermediate
  • Duration: 60 Min

recorded version

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

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: +1-650-565-8542


Read Frequently Asked Questions

This FDA compliance training will explain how to measure and reduce the FDA recordkeeping burden.

Organizations seeking to improve quality, productivity and compliance in their FDA-regulated activities must streamline the process of creating policies and procedures. This seminar will explain how to measure and reduce the FDA recordkeeping burden.

What Attendees will Learn:

  • What the document lifecycle is and how much it "costs"
  • How to calculate the costs of the document lifecycle
  • Strategies for managing documents and content
  • Practical tips to start reducing the recordkeeping burden today

Who Will Benefit:

  • Supervisors and Managers
  • Manufacturing and Validation personnel
  • Lab and Regulatory Associates
  • Consultants and Contractors

Instructor Profile:

Chris Whalley, is a content management strategist focusing on FDA-regulated industries. The founder and publisher of Doxpub, Inc. (, 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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