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.