This objective of this seminar is to provide participants with an understanding of:
This seminar is intended for non-statisticians and will furnish participants with tools to understand statistical terminology and methodology in clinical trials. The presentation will focus on actual case studies as they relate to regulatory requirements (FDA, EMA and EU). There is no statistical prerequisite for this seminar.
Following titles and departments who are involved with the statistical aspect of clinical trials, in order of bio-statistic’s will be benefited by attending this seminar:
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