This webinar was successfully completed on May 16, 2013. To receive information on this webinar or any of our upcoming webinars, please visit the following link:

Webinar Date
16 May, 2013 11:30 AM (EST)

Main focus on

Regional advantages
Patient enrollment
Regulatory challenges
Case studies


  • Introduction
  • Medical Device history in CEE
  • Medical device classification
  • Clinical Trial Application
  • Case studies

Éva Reif MD
CRM, HungaroTrial CRO

Dr. Eva Reif is a Clinical Research Manager at HungaroTrial. She received her degree from Semmelweis University in Hungary and made large strides in the medical field working as an anesthesiologist at a heart and vascular surgery center. Since then she has spent 14 years in the clinical research industry working for Bristol-Myers Squibb and Sanofi. Dr. Reif has now been with HungaroTrial for two years where she has developed and managed every medical device project since her arrival.

Do you know;

WHY are more medical device companies looking to conduct first-in-man and pilot studies in the region?
HOW can medical device research projects succeed in the region?
WHAT are the main regulatory challanges?

Our webinar will answer these questions and address many other important topics, such as regulatory application requirements, a global comparison of study capabilities, and the different medical device classifications.
Clinical Research Manager of HungaroTrial, Dr. Éva Reif, will share her knowledge and experiences with you on these and other topics.

Register for this Webinar

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    Best regards,
    HungaroTrial Team