SafetyDrugs is a new adverse event reporting system that supports the capture, management, reporting and analysis of adverse event of all medical products: from drugs to devices, from biologics to vaccines.

Our system is compliant with ICH, EMEA and FDA rules and supports both MedDRA and WHO-Drug dictionaries.

While a lot of adverse event reporting systems needs several month to be operative, thanks to the validation document set included in our offer, SafetyDrugs can be ready to use in just one month. Moreover the possibility to access it via SaaS (Software as a Service) and a small price make SafetyDrugs one of the most cost effective products on the market.

None is too big: we know that big companies often have big necessities, that’s why SafetyDrugs can be fully customized, from workflow to site parametrization, to meet company needs. Furthermore our business intelligence is the perfect solution to deal with a vast amount of data from adverse events to perform signal detection.

…or too small: our easy to use interface and possibility to access SafetyDrugs via SaaS (Software as a Service) make it suitable for small companies with less than 10 cases every year.