NEW Online Series!
Advanced Topics in LC Method Validation
Presented by Dr. Michael Swartz
Research Director for Synomics Pharma
REGISTER TODAY!
New Interactive Seminars!
| 1. |
Analytical Instrument Qualification
**Live Event Completed**
Access to presetnation On-Demand Digital Archieve Available for Immediate Viewing/Download |
| 2. |
Design and Implementation of LC Robustness
Friday, September 14, 2007
11am – 12pm ET |
| 3. |
Validating LC Impurity Methods
Friday, October 12, 2007
11am – 12pm ET |
| 4. |
Adopting New Technology in a Regulated Environment
Friday, November 9, 2007
11am – 12pm ET |
| 5. |
Investigating Out of Specification (OOS) Results
Friday, December 14, 2007
11am – 12pm ET |
| 6. |
Analytical Method Transfer
Friday, January 11, 2008
11am – 12pm ET |
Save 25%
When you sign up for all six sessions!
Groups, site licenses, and single sessions available.
Call 800.234.4535 or visit www.ivthome.com for more details.
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| • |
Live Multi-Media Presentation |
| • |
Live Q & A |
| • |
Certificate of Attendance |
| • |
Access to the On-Demand Digital Archive |
| • |
PDF Copy of Presentation Slides |
WHO SHOULD ATTEND?
- Directors
- Lab Managers
- Practicing Chemists
- Scientists
...in regulated laboratories responsible for designing
or implementing method validation protocols with
an LC focus
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OUR EXPERT PRESENTER
Michael Swartz, Ph. D.
Research Director for Synomics Pharma
Dr. Swartz, Research Director at Synomics Pharma, has been involved in liquid chromatography (LC) instrument, market, and business development, and has consulted, taught courses and lectured on method development and validation worldwide for over 25 years. He is the author of several books and book chapters, over 50 manuscripts, four patents, and has presented over 175 contributed and invited papers at various technical symposia around the world. He has served on the Scientific Editorial Advisory Board of LC/GC Magazine since 1998, where he co-authors the popular Validation Viewpoint column.
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