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EVENT DATE
Dec 2017
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Biostatistics for Non-Statisticians in Pharma and Medtech

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Overview

This objective of this seminar is to provide participants with an understanding of:

  • Basic principles of bio-statistical thinking and methodology
  • Design and analysis of clinical trials
  • Techniques for increasing trial efficiency with an eye to reducing costs and increasing chance for success

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.

 

Who will Benefit:

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:

  • Departments: Clinical, Regulatory, R&D, Marketing
  • Clinical Titles: Medical Director, Director of Clinical Affairs, VP Clinical, Clinical Manager, Clinical Department Manager, Clinical Project Manager, Clinical Staff, CRA (Clinical Research Associate), Study Coordinator
  • Regulatory Titles: VP Regulatory Affairs, Manager of Regulatory Affairs, Regulatory Scientist
  • R&D Titles: Director of R&D, VP R&D, R&D Project Manager, Engineers, Quality Engineer, Algorithm Developer

 

Note: Use coupon code REFERRAL10 and get 10% off on registration.

For Registration:

http://www.complianceonline.com/biostatistics-for-non-statisticians-in-pharma-medtech-seminar-training-80517SEM-prdsm?channel=eventsinamerica

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