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Pharmaceutical Production Batch Record Review
in Berlin from 03.12.2012 - 04.12.2012This course is designed for pharmaceutical production, quality assurance, and compliance personnel who are responsible for the review and audit of production batch records, and batch record deviation investigations. The purpose of this course is to take the mystery out of the batch record review process. The class examines the FDA and EU regulatory requirements for documentation and batch record reviews, explains the elements of the batch record review process, and clarifies the pathway to effective deviation investigations.
| Event Date: | 03.12.2012 to 04.12.2012 | |
| Event Location: |
The Berlin Hilton
Berlin Germany |
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| Event Organiser: |
Center for Professional Innovation & Education, Inc.
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