Event Date/Time: Sep 30, 2008
It explains how to create documentation that will meet regulatory requirements worldwide. It describes how to determine the right amount of validation documentation for a system and which documents to create to maximize efficiency. It also covers proven techniques for creating documents that meet regulatory requirements
Areas Covered in the seminar:
* Understand GAMP and FDA requirements.
* Understand what does and does not need to be validated.
* Learn which documents to use for different validation requirements.
* How to create documents efficiently.
Who will benefit: