Post-graduate qualification
| 2010 - 2011 | GMP: Manufacturing and quality control of clinical study material according to relevant guidelines (Cirqum) |
| 2009 - 2011 | Several internal training courses related to various aspects of the conduct of studies at a Clinical Research Organisation (CRO) specialising in aerosol medicine and radiolabelling (Inamed) |
| 2006 – 2012 | Training as auditor (IHK, MedPharmTec, DGPharMed) |
| 2004 - 2010 | Professional Development Program of the European Medical Writers Association EMWA, >30 workshops 2005 - 2009 Advanced certificate 2005 - 2009 Multidisciplinary foundation certificate 2004 - 2005 Foundation certificate, specialised area “drug development” |
| 1998 - 2005 | Continuous training as clinical research associate (ICH-GCP) at three CROs (Kendle, Harrison, MedPharmTec) |
| since 1998 | >30 training sessions related to various aspects of the regulatory environment and to the conduct of clinical studies and non-interventional observational studies of drugs and medical devices in humans (BVMA, DGPharMed, Forum, Harrison, IIR, Inamed, Kendle, MedPharmTec, MEGRA, Vicron) |
| 1996 – 1997 and since 2013 | In vivo biodistribution and pharmacokinetic studies, i.e. animal experimentation, handling of radioactive materials (Technical University, Munich, and GSF-National Research Center for Environment and Health, Neuherberg, Germany) |
CV and all certificates available upon request.