Mastering IVD Clinical Trials: Basic Statistics for IVD Trials

This eConference is the third in a four-part series presented by renowned experts Dr. Cheryl Hayden and Dr. Robert Thiel.  

Why should you take this eConference?
To determine the best approach to the statistical analysis of IVD data for FDA approval

You will receive:
- Slides
- An expert speaker
- A chance for Q&A
- CEUs & Certificate

Who should attend:
Anyone who will be involved in IVD clinical trial design and management, such as:
- In vitro diagnostic Manufacturers
- Product Managers Regulatory
- Affairs Managers
- Project Managers
- Sponsors
- Monitors
- Regulators
- CRO personnel
- IRB personnel
- Laboratory personnel

Presenter:
Clinical Device Group is proud to present Dr. Robert P. Thiel. Dr. Thiel has degrees in physics, clinical counseling and psychometrics. He is an expert in the analysis of IVD data for the Medical Device Industry with more than 75 510K and 5 PMA approvals. He has published papers in the area of free PSA, Breast Cancer, Ovarian Cancer, Liver Disease and multivariate analyses as applied to sports (baseball and basketball). His current interests lie in the area of bootstrap and permutation test methodology and the application of these methods to small sample trials. Dr. Thiel can be contacted at rpthiel@thielstatcon.com.

The purchase is $401 for the CD. Event materials are available on the CD itself. Each attendee is eligible for 0.15 CEUs upon completing the course feedback via the link provided with the event materials. Click here to purchase.