Overview:In this two-day seminar, you will learn how to configure your Excel application with the features required for 21 CFR part 11 compliance, helping you to avoid 483s. Using the risk-based computer system validation approach, you will validate your own Excel application. Use of the validation templates is necessary and important because it typically saves two-thirds of the validation time and costs. This seminar will improve your Excel skills and create a set of validation documents that you can use for subsequent Excel application validation projects.Who Will Benefit:Executives/Managers within Dietary Supplement or Natural Product companiesRegulatory Compliance Professionals in the Supplements or Natural Products areaQuality Assurance or Quality Control ProfessionalsDietary Supplement or Natural Product Manufacturers & DistributorsSales/Marketing Personnel in the Supplement or Natural Product IndustriesDay 1 - 21st February 2013Lecture 1: Introductions  Lecture 2: Regulations for Electronic Records  Lecture 3: 21 CFR Part 11 - Electronic Records & Signatures  Lecture 4: The Risk-Based Validation Approach  Lecture 5: Excel Applications - part 1Day 2 - 22nd February 2013Lecture 6: How to Conduct a Hazard Analysis/Risk Assessment  Lecture 7: Excel Applications - part 2Lecture 8: Main Concepts to Remember Lecture 9: &ALocation : San Francisco | February 21st & 22nd, 2013 (Thursday & Friday)Price: $1,295.00GlobalCompliancePanel Event CoordinatorToll free: 800-425-9409Fax: 302-288-6884