Accovion Plus
Accovion Plus
EuropeanDoorOpener
Accovion’s EuropeanDoorOpener provides modular service solutions designed to support your small- or medium-sized pharmaceutical, biotechnology or medical device company in all aspects of your European development program. Read more
Patient safety narratives
Guidelines issued by regulatory agencies and the International Conference on Harmonization (ICH E3 and E6) define stringent sponsor responsibilities for safety assessment and reporting in clinical studies, including narrative statements on special categories of adverse events for individual subjects. Accovion’s expert medical writers in cooperation with the project team can produce detailed patient safety narratives tailored... Read more
Archiving of clinical data
Accovion is able to archive your clinical data, for example for closed studies in clinical databases. For this purpose, we apply our proprietary archiving approach based on the CDISC Operational Data Model (ODM). Read more
Sonja Riebel, BSc
Manager Marketing & Communication
+49 6196 7709-339
