Mastering IVD Clinical Trials: Multiple Endpoints in IVD Trials

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

Objective:
In this eConference we will discuss issues that affect the validity and utility of the data collected in an IVD Clinical Trial, and how to avoid pitfalls that would adversely affect data collection and analysis. We will also discuss methods of increasing the efficiency of the clinical trial.

Why should I take this eConference:
Attending this eConference will help you design a clinical trial that is effective and efficient, and help you avoid common errors in IVD trial design.

You will learn:
You will learn how to optimize use of a gold standard, how to design a trial to allow multiple endpoints and uses of the data, and how to include multiple assays in a single trial.

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

You will receive:
- Slides
- Relevant articles by the presenter
- An expert speaker
- A chance to liten to other's QnA
- CEUs & Certificate

Presenter:
Clinical Device Group is proud to present Dr. Cheryl Hayden. Dr. Hayden has degrees in medical technology, biostatistics, and microbiology. She has worked for 25 years in the field of clinical research, 8 years in a consulting capacity. Much of her experience is with in vitro diagnostics. She was involved in early work with tumor markers, determining the utility of these assays and raising awareness of their use in the oncology community. She has published several papers on trial design for IVDs, specifically on nested endpoints and flaws of gold standards. Dr. Hayden’s interest in IVD trial design stems from her early training in medical technology. Dr. Hayden can be reached at Cheryl.hayden@comcast.net.

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.