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.
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...
Our highly skilled IT staff has long-standing experience in clinical IT solutions and in all relevant architectures. We will make this available for you to support your own strategic IT projects.