The International Regulatory Affairs Network
FDA Inspections of Clinical Data Systems
26.04.2010 - 27.04.2010
Ort: Dublin, Ireland
The course will provide the tools needed to prepare for a Clinical Data System inspection and to assess risk areas that need prioritization.
This course explores the preparation for FDA systems inspections focusing on establishing a new program or seeking improvements in an ongoing quality initiative. The course provides practical information for improving presentation and substance of Clinical Data Systems documentation in anticipation of a FDA Inspection. In addition, the course will address critical issues and potential observations resulting from a Clinical Data Systems audit. Topics include the following: inspection fundamentals; computer validation and Part 11 inspection concerns; assessing standard operating procedures; assessing system documentation; preparing for the inspection; and maintaining compliance.
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http://www.cfpie.com/showitem.aspx?productid=034&source=swissbio
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