To ensure reliable and timely pharmacovigilance reporting we have established efficient processes. All employees are regularly trained in this respect. As a matter of course, we consider the specific business processes of our clients.

In all projects for clients from the pharmaceutical industry, we implement a close pharmacovigilance monitoring so that information on any events that are subject to reporting can be forwarded to our clients on the same day. Our reconciliation processes ensure comprehensive documentation.

emphasis is committed to complying with local laws, regulations, industry codes of conduct and other guidelines regarding the reporting of adverse events in pharmaceutical market research projects.