Efficient Batch Record Review 29-30 April 2010 Barcelona, Spain Please click here to view the program of this conference or course To book for this program, just click on the option: Book this option: Non-ECA Members (EUR 1690,--) Book this option: ECA Members (EUR 1521,--) Book this option: EU GMP Inspectorates (EUR 845,--) Book this option: APIC Members (does not include ECA membership) (EUR 1605,--) Book this option: QP Association Members (EUR 1521,--)
At this conference we offer a Conference Exhibition. Please click here in order to view the registration form (PDF) for exhibitors.
Learning Objectives During this course, you will learn all relevant aspects to conduct and to improve your system of the Batch Record Review which fulfils GMP requirements. Furthermore, you will get to know possibilities and tools to increase efficiency and decrease costs at your company. Background The Batch Record Review is an essential tool for assuring the quality of a pharmaceutical process. Various regulations and guidelines address this topic for the pharmaceutical industry and it is a very important step before a product can be released by a Qualified Person. However, over the years, documentation has become more and more extensive and the review can be very time-consuming. During this Education Course, experts from the pharmaceutical and API industry will cover all relevant aspects helping you to improve your batch record review. An optimised batch record review will also enable you to improve your process capabilities. Furthermore, many observations made in inspections relate directly to the review of documents. This fact clearly demonstrates the importance and challenge of implementing a GMP/FDA-compliant Batch Record Review.