We offer you an absolute professional support at study start and during the conduct of the clinical trials.
The right site selection and a fast submission process to the Health Authority and Ethics Committee as well as the profound knowledge in the area of contract negotiation will guarantee you an early study start in Austria and therefore an advantage in comparison to other European countries.
We offer you the full project management for non interventional studies (NIS) including sites visits if required.
We are able to support you during an audit and/or inspection preparation phase as well as afterwards during the corrective and preventive action plan implementation. Our support is based on more than 15 years of audit and inspection experiences including FDA.
Ingrid Kuhn, M.D.
M.D. June 2007 Medical School University Vienna
|July 2014||-||ongoing||Owner (CEO) / IK-MED e. U.|
|April 2010||-||June 2014||Clinical Research Director|
|April 2008||-||April 2010||Head of Clinical Operations|
|January 2003||-||March 2008||Head of Medical Affairs|
|July 1998||-||December 2002||Medical Manager|
|November 1992||-||June 1998||Clinical Trial Project Leader|
|October 1990||-||October 1992||Clinical Research Associate|
|October 1979||-||September 1990||Medical Assistant|
Nina Derkits, MSc
2008 Master’s Degree in Biomedical Engineering Sciences, University of Applied Sciences FH Technikum Wien
|2017||-||ongoing||Project Lead Clinical Research / Medical Affairs|
|2014||-||2016||Clinical Research Manager|
|2010||-||2014||Clinical Project Manager|
|2008||-||2010||Clinical Research Associate|