SOHInfo’s AI-based Surveillance daily monitors literature repositories and adverse event databases worldwide to keep you updated on potential issues with your product(s) – as well as your competitors’ products.
Surveillance lets you select from a wide range of data sources to continuously monitor what is being published and reported for any product or group of products.
Receive notification each time a selected product or group of products appears in a literature publication or reporting database. The system actively monitors and interprets literature and adverse event databases and generates alerts based on identified triggers, such as case studies (ICSR) or severity and frequency of adverse events.
Using powerful AI algorithms, Surveillance monitors the sources used by regulatory agencies providing real-time trends and insights. With daily notifications about potential issues you can proactively address problems arising from reported AE’s and published articles. It also provides a solid basis to satisfy Post Market Surveillance requirements under most regulatory agencies.
Full Coverage of the published literature and adverse event reporting databases:
EU Clinical Trials
Setup notification and alerts based on selected events, including:
– Number of Reported Events
– Reported Events by Severity
– Reported ICSR’s in the Literature|
– Comparisons of all Products
– Rate of Publication from all Sources
– Complete Literature Breakdown