Device Trials in Central/Eastern Europe

Why take this eConference?
You will get practical knowledge and helpful hints in using Central/Eastern Europe to accelerate study start-up, maximize enrollment and obtain high quality data.

Objective:
To describe the benefits and challenges of conducting device trials in Central and Eastern Europe using Poland and Ukraine as examples.

Who should attend:
- Device Manufacturers
- Regulatory Managers
- Clinical Operations and Project Managers
- Site Monitors
- CROs

You will learn:
The structure and functions of the Regulatory Authorities in Poland and Ukraine as they apply to the approval of device clinical trials. Topics will include:

- The regulatory approval process, timeframes, prioritization of activities and required documents.
- How to construct site Agreements to minimize delays in this process.
- How health care delivery in these countries may impact study participant recruitment.
- What to expect in the way of data quality.
- Useful nuts and bolts of information.

You will receive:
- Slides
- An expert speaker
- A chance to listen to other's Q&A
- CEUs & Certificate

Presenter:
Clinical Device Group is proud to present Peter Goodenow, Vice President, Clinical Operations, PharmaTrials-Polska Sp. z o. o. PhamaTrials is a Contract Research Organization located in Warsaw, Poland, specializing in conducting device, diagnostics and drug clinical trials in Poland and other Central and Eastern European countries. Mr. Goodenow can be reached at Peter.Goodenow@PharmaTrials.info.

The purchase is $420 for OnDemand access and $470 for the CD. Event materials are available by download for OnDemand or are 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.