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.
Here is a taste of what you will uncover in this informative session:
Who Should Attend
This webinar is applicable to everyone in the life sciences industry, especially:
Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.
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....
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