About us

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.

LinkedIn

Education

M.D. June 2007 Medical School University Vienna

Languages

German English

Work experience

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

LinkedIn

Education

2008 Master’s Degree in Biomedical Engineering Sciences, University of Applied Sciences FH Technikum Wien

Languages

German English

Work experience

2017 - ongoing Project Lead Clinical Research / Medical Affairs
2014 - 2016 Clinical Research Manager
2010 - 2014 Clinical Project Manager
2008 - 2010 Clinical Research Associate