Apply a Global Quality Standard to Life Sciences Compliance Documentation

Event Information
Product Format
Live Webinar
Presenter(s)
Conference Date
Add to my calendar   Fri, Jun 22, 2018
Aired Time
1 pm ET | 12 pm CT | 11 am MT | 10 am PT
Length
60 minutes
Product Description

Learn the Very Real Value of Standardized Documentation


Your life sciences organization may have a number of individuals who pull compliance documentation information and compile it into usable data. But if your documentation standards are not written in stone, you could be getting buckets full of data that lack synthesis and harmony. In short, you could be making a mess that will take forever to untangle while key details fall through the cracks.

Don’t make this common mistake. Join technical documentation consultant Charles H. Paul in this live webinar to learn the true purpose and function of regulatory documentation in the life sciences industry. He will show you what pitfalls you can run into, how to avoid them, and how to create an effective documentation development process.

You’ll leave this event understanding the true value of standardized compliance documentation, how to avoid the pitfalls associated with writing regulated documentation, how to apply the global documentation standard to quality management, why harmonization across borders is important, which documentation formats to use, and how to use subject matter experts. Learn today how to develop an effective documentation development process that will put you on solid footing.

Session Highlights

Here is a taste of what you will uncover in this informative session:

  • The true purpose and function of regulatory documentation
  • What the “value add” is
  • The pitfalls associated with writing regulated documentation
  • The global documentation standard as it relates to quality management
  • Harmonization across borders and why it is important
  • Documentation formats
  • How to gather the technical information you need
  • Using Subject Matter Experts
  • Effective documentation development processes

Who Should Attend

This webinar is applicable to everyone in the life sciences industry, especially:

  • Operations managers and directors
  • Compliance managers and directors
  • Training managers and directors
  • Quality assurance managers and directors
  • Documentation specialists

Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.

Order Below or Call 1-866-458-2965 Today

You can also order through:
Phone

1-866-458-2965

Fax

1-919-287-2643

About Our Speaker

Charles H. Paul

Charles H. Paul is the President of C. H. Paul Consulting, Inc. – a regulatory, training, and technical documentation consulting firm. Charles is a management consultant, instructional designer and regulatory consultant and has led C. H. Paul Consulting, Inc. since its inception over 25 years ago. He regularly consults with Fortune 500 pharmaceutical, medical device, and biotechnology firms assisting them in achieving human resource, regulatory, and operational excellence....   More Info
More Events By The Speaker

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