<img src="https://ws.zoominfo.com/pixel/OJkQgdjSvoid2NFoB5Qs" width="1" height="1" style="display: none;">
Jon Ingi Bergsteinsson-2-1

The MDR is forcing many MedTech companies to conduct clinical studies to gather data for Post-Market Clinical Follow-Up (PMCF) and clinical evaluation.

One of the first crucial steps in designing a clinical study is determining the number of subjects to recruit i.e the study sample size.

To pass scrutiny from Notified Bodies on PMCF and clinical investigation plans, you have to justify sample size estimation with scientific reasoning.

In this webinar you will learn:

  • The basic inputs behind sample size estimation
  • How study design can impact sample size
  • How to prepare for a discussion on sample size with a statistician


Medical Device, Clinical Study, Sample Size


MEDIE 2018 WEB 29344 copy 2


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Jón I. Bergsteinsson
VP of Global Business Development 
Oren Bar-Ilan
Managing Partner



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