Versed in global regulations, we ensure study compliance
All studies managed and designed by ZEG Berlin comply with current global pharmacovigilance regulations. Fully trained in European and United States pharmacovigilance regulations, our staff receive annual training on the changes occurring in the European, the US and global pharmacovigilance environment. We design PASS ensuring that studies are compliant with GVP and providing study sponsors with the information they require. Our pharmacovigilance team assesses all adverse events reported in the course of a study for validity prior to undertaking the appropriate reporting processes within the given time limits. If you would like to understand more about our pharmacovigilance practices within our studies, we would be happy to talk to you further.