Your benefits at a glance
Planning – Planning of your clinical studies to comply with the methods currently required by drug approval authorities and regulatory boards (e.g. the German Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen, IQWiG)
Full-CRO-service – Design and execution of your studies in accordance with GCP using Oracle Clinical and Oracle Clinical RDC 4i
CSG as intermediary - Strengthening of your position in, and products for, the health care sector through interaction with other interest groups.
Training – Improvement of your method and system competence both for internal use as well as vis à vis prescribers and users of your product
Review – Critical analysis of available data on your product or on products in the relevant market segment
Related analyses – Epidemiologically based analyses of the market with regard to reimbursement issues.