This webinar was successfully completed on May 22, 2013. To receive information on this webinar or any of our upcoming webinars, please visit the following link:

Webinar Date
22 May 2013 11:30 am EST

Main focus on

Regional development
Submission protocol
Regulatory challenges
Case studies


  • Introduction
  • Development of paediatric study regulations
  • Submission challenges
  • Paediatric studies in CEE
  • Case studies

Klaus Rose M.D., M.S.
Chairman, DIA Pediatric SIAC

EFGCP Children’s Medicines Working Party

IFPMA Pediatric Task Force

Dr. Klaus Rose is chairman of DIA Pediatric SIAC He has held various positions in R&D and medical affairs of progressive responsibility culminating in the position of Global Head Pediatrics at Novartis and Roche. His main interest is the regulatory and ethical background of the pediatric clinical trials; planning and implementing pediatric projects.

Do you know;

WHY are paediatric trials difficult to initiate?
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 including, tightening paediatric regulations and PIP submission issues.
Dr. Klaus Rose, chairman of DIA Pediatric SIAC, will provide insight and knowledge concerning these subjects.

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