Training Course Syllabus:

Good Documentation Practices

Why Should you Attend:

"Good documentation practices" is a "current" industry practice that is reviewed and cited by federal regulators when audited. Pharmaceutical/Biological document are legal documents that are controlled by all regulatory agencies. The person or persons responsible for filling out these documents accepts the consequences if the documents are not filled out according to good documentation practices. Good documentation practices are expected to assure they are accurate, legible and traceable to name a few. The lack of such good documentation practices are routinely cited in FDA 483 observations. Attend this webinar to learn proper methods for documenting data in the highly regulated pharmaceutical industries.


You will take away a better understanding of how project management can assist you in performing your role in your organization.

Objectives of the Presentation:

Seminar Summary:

This webinar will cover the basics of what good documentation practices include, along with examples of practices not acceptable to auditors. This webinar will help attendees review their own procedures and what should be included in applicable training sessions for new employees along with refresher training for those who are more experienced. (see full course description)

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