About ECRON AcuNova   Vision and Quality policy   Letter from Leaders      Letter from Vice Chairman      Letter from President   The Team   Fact sheet     Team at ECRON AcuNova Europe     Mr. D.A Prasanna   Dr. K.D Wiedey   Dr. Kohkan Shamsi   The Team at Manipal AcuNova India   Team at ECRON AcuNova Europe       Dr Sabine Kuehnau has been with ECRON since 1992, actively involved in the Company development from a national to an international full-service CRO. She is responsible for proposal management as per client needs in the pharmaceutical, biotech and device industry. In addition, she overlooks the supervision of project performances, cost control, personnel affairs and day-to-day business. Dr Kuehnau has managed more than 100 national and multi-national clinical projects (mainly phase II - phase IV), performed mainly in Western and Eastern Europe. The key areas include rheumatology, gastroenterology, gynecology, pulmonology, dermatology, cardiovascular diseases etc.   Prior to ECRON, Dr Kuehnau began her career in 1991 as a medical writer. In addition, since 2005, she has been the Production Manager according to AMG (German Drug Act) and Managing Director of ARCUS Pharma Consult since 1997.   Dr Kuehnau is a member of the German Society for Pharmaceutical Medicine (DGPharMed) and the Association of Clinical Research for the Pharmaceutical Industry (ACRPI). Dr Kuehnau is an MSc in Biology and was awarded a PhD by the Faculty of Biology of the University of Constance (Germany).       Dr Schiewe has been with ECRON since 1993. Having joined as a Clinical Research Associate, her exemplary performance quickly involved her with project management functions in 1995, after which she rose to being Director Clinical Research from 1999 onwards. She has been critical in expanding the ECRON partner network all over the world. Dr Schiewe's managerial and team leading skills predestine her for the supervision of project performance, cost control and manpower management. Dr Schiewe has supervised about 50 multi-national clinical trials (phase II - phase IV) in Western and Eastern Europe as well as in South America. Some key areas include oncology, heart and vascular diseases, gastrointestinal diseases and hormone replacement therapy.   She had been working as an Assistant Lecturer at the chair of phytopathology of the University of Constance before she joined ECRON. Dr Schiewe is a member of the German Society for Pharmaceutical Medicine (DGPharMed). She is an MSc in Biology and was awarded a PhD by the Faculty of Biology of the University of Constance (Germany).       Dr Schaefer is the Head of Quality Assurance Unit since 1995. Having joined ECRON in 1990, Dr Schaefer has gained thorough experience in the various aspects of clinical trials of medicinal products in human subjects and took over to quality assurance functions. She was instrumental in implementing ECRON Standard Operating Procedures in compliance with ICH GCP standards on a global level and on national levels in Europe as well. As a trained auditor, she has successfully been an independent GCP auditor in international trials in and outside Europe. Dr Schaefer is a member of the German Society for Good Research Practice (DGGF).   Prior to joining ECRON, Dr Schaefer had been working in the R & D division of Byk Gulden Lomberg in Constance. Dr Schaefer has completed the study of veterinary medicine at Justus Liebig University in Gießen and was awarded a PhD by the Faculty of Veterinary Medicine of the Free University in Berlin       Dr Bluemner has been with ECRON since 2001. With over 25 years enriched experience in Clinical Research, he is responsible for various aspects in the project progress namely planning, data management, statistics and medical writing. Dr Bluemner has provided biometrical guidance for numerous multi-national clinical trials (phase II - phase IV) in Western and Eastern Europe as well as in South America. The key areas include oncology, heart and vascular diseases, gastrointestinal diseases, skin diseases, and hormone replacement therapy.   Prior to ECRON, he had been with Max Planck Institute for Plasma Physics as Data analyst and programmer in Garching (Germany) and as Director Biometrics at Staticon International in Martinsried (Germany). Dr Bluemner is a member of the German Society for Medical Informatics, Biometrics and Epidemiology (GMDS) and the International Biometric Society. He is also a member of the Drug Information Association (DIA). In 1993 he was awarded with the E.W. Baader prize in Industrial Medicine.   Dr Bluemner is an MSc in Mathematics and was awarded an MD by the Ludwig Maximilian University in Munich (Germany). < back

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