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GlobalCompliancePanel, Online
March 4, 2010
Learn how to select, conduct and document the right tests in the right sequence. High Performance Liquid Chromatography is the most frequently used analytical tool for pharmaceutical and API testing laboratories. FDA and international agencies require HPLC equipment to be calibrated, qualified and tested to ensure accurate and reliable analytical results. Even though this is well known since long time, laboratories are unsure on what exactly should be tested initially and on an on-going basis. The main challenge is to do the right testing in the right sequence.
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Organized by:
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GlobalCompliancePanel |
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Invited Speakers:
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Dr. Ludwig Huber Chief Advisor - Global FDA compliance, Agilent Technologies
Ludwig Huber, Ph.D., is Director of Labcompliance and Chief Advisor for global FDA compliance at Agilent Technologies. He is the editor of Labcompliance, the global on-line resource for validation and compliance issues for laboratories. He is the author of the books "Validation and Qualification in Analytical Laboratories, and "Validation of Computerized Analytical and Networked Systems", Informa Healthcare.
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Deadline for Abstracts:
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March 2, 2010
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Registration:
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Thursday, March 4, 2010 10:00 AM PST | 01:00 PM EST | | Live live online training only for one participant | | |
| | Corporate Live 4 to 10 participants from a single location (For multiple locations contact Customer Care) | |
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E-mail:
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webinars@GlobalCompliancePanel.com
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