Webinar on "Statistics for Quality Control and Process Validation: Comparing Sets of Data" from GlobalCompliancePanel
When preparing statistics for Quality Control and Process Validation, professionals are required to compare various sets of data. In this series on this topic, the expert, Dr. Steven Kuwahara has already covered the area of converting the process for comparing two sets of data.
- Fresno, CA (1888PressRelease) January 22, 2013 - When preparing statistics for Quality Control and Process Validation, professionals are required to compare various sets of data. In this series on this topic, the expert, Dr. Steven Kuwahara has already covered the area of converting the process for comparing two sets of data.
In this particular webinar, he will take up the issue of what happens when more than two sets of data are needed for comparison. This question will be at the core in this series of webinars that Dr. Kuwahara will be conducting. In this webinar, he will offer simple and practical methods of dealing with comparison of two or more sets of relatively uncomplicated data.
What is imparted here at this session will serve as the basis for a higher understanding of more advanced studies on more complex data sets. Hence, this session will serve as the continuum of the levels of difficulty in dealing with multiple data sets that this series will cover.
This webinar will cover the following areas of study:
o The paired t-Test
o Snedecor's F - Test
o A one factor, one level, ANOVA
o Identifying the unusual result
o The Least Significant Difference and Duncan's Multiple Range test
When:January 22, 2013, 10:00 AM PDT | 01:00 PM EDT
By whom:
Steven S. Kuwahara, Ph.D., is the founder and Principal of GXP BioTechnology LLC, a consulting firm that works in the areas covered by the GLP and GMP of drugs, biologics, and nutraceuticals. After securing degrees in Biochemistry from Cornell and the University of Wisconsin, Steven started off as an Assistant Professor of Chemistry. His testing skills were honed in the initial years of his career at the Division of Biologic Products at the Michigan Department of Public Health (now BioPort Corp.), where he became the head of Quality Control. Here, he developed expertise in the testing of blood derivatives, viral and bacterial vaccines.
His work has also dealt with all aspects of GMP and GLP in relation to biopharmaceuticals. He has worked with small molecules, proteins, cells, and gene therapy vectors.
During an impressive career spanning over 30 years, Steven has applied his academic knowledge to quality control in the pharmaceutical industry. Steven has written several papers and book chapters, and serves on the editorial advisory boards of BioPharm, BioQuality, and the Journal of GXP Compliance. He has held certifications as a CQA, CQT, and CQE from the American Society of Quality and was certified (RAC) by the Regulatory Affairs Professionals Society.
For whom:
The webinar will benefit
o Regulatory Affairs personnel who prepare the CMC sections of submissions
o Development personnel who will set the early specifications
o R & D personnel who will contribute data for use in development
o Project managers for product development studies
o Quality systems auditors
o Consultants
Duration: 90 minutes
To enroll for this webinar, contact
webinars ( @ ) globalcompliancepanelcom
Phone: 800-447-9407
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