SOHInfo’s AI-based Post Market Surveillance regularly ingests data and information from literature repositories, adverse event databases worldwide, and social media to keep you updated on potential issues – for your, and your competitors’, products.
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, reporting database, or on social media. The system generates alerts based on identified triggers, such as case studies (ICSR) or severity, type, and frequency of adverse events.
Using powerful AI algorithms, data from sources used by regulatory agencies are analyzed to provide real-time trends and insights. With notifications about potential issues you can proactively address problems arising from reported AE’s and published articles. The systems 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:
Continuous Monitoring:
Medline
Embase
WHO
EU Clinical Trials
MAUDE
FAERS
VigiBase
EudraVigilance
Twitter
LinkedIn
Facebook… and Others
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