Interactive, educational web seminars. It’s simple: pick the event you want to purchase access to. We will email you reminders of the time and date. Then just log on and experience global industry leaders presenting conference quality content on today’s hot topics without leaving your desk.

Your Purchase Package Includes:

• Access to the Live Event
• PDF copy of the presentation slides
• Certificate of Attendance

Tuesday, March 11, 2008
12:00pm-1:00pm ET
FDA Inspections: What to Expect
Gamal Amer, Ph.D.,Senior Director Compliance and Validation Services: BE&K BioPharm
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Tuesday, March 11, 2008
6pm-7pm ET
Simple, Effective, compleX sample analYsis by using comprehensive two-dimensional gas chromatography – (SEXY-GC×GC)
Professor Philip J. Marriott, Australian Centre for Research on Separation Science, School of Applied Sciences, RMIT University, Melbourne Australia
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Thursday, March 20, 2008
11:00am – 12:00pm ET
Current FDA 483s and Warning Letter Trends With an Emphasis on Emerging Global Trends
Gaurav Walia, M.S.,Assistant Director of Laboratory Operations and Administration in Pharmaceutical Research and Development: Forest Research Institute
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Tuesday, April 1, 2008
11:00am-12:00pm ET
Standardization of Instrument Qualification, Re-qualification and Calibration in Pharmaceutical Research and Development Laboratories
Gaurav Walia, Assistant Director of Laboratory Operations and Administration in Pharmaceutical Research and Development at Forest Research Institute
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Thursday, April 10, 2008
11am – 12pm ET
A Statistical Basis for Quality by Design
Lynn Torbeck, Principal Consultant
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Wednesday, April 16, 2008
12:00pm-1:00pm ET
FDA Inspections: How to Prepare
Gamal Amer, Ph.D., Senior Director Compliance and Validation Services: BE&K BioPharm
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Thursday, April 24, 2008
12pm to 1pm ET
Validating Prepackaged Eluents for HPLC Applications
Mr. Bryan E. Bell, Quality Assurance Representative, Eli Lilly & Co.
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Wednesday, April 30, 2008
12:00pm-1:00pm ET
483’s & Warning Letters: Developing an Effective Integrated Response
Patrick L. DeVillier, M.S., Senior Director, Compliance, A.P. Pharma
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For questions or more information please contact Jamie Carpenter at
jcarpenter@advanstar.com or call 800-234-4535