Reducing the Cost of Creating Documents for FDA-Regulated Industries
Instructor:
Chris Whalley
Product ID: 700126
Training Level: Basic to Intermediate
- Duration: 60 Min
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
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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