IntelliVigil is a Next-generation , integrated and complete pharmacovigilance solution for pharmaceutical, biopharmaceutical and medical device companies. IntelliVigil is built on a big data frame work. This brings in new capabilities in handling large volumes of data, system response and ability to handle variety structured and unstructured data.
Pharmacovigilance regulatory intelligence to help companies maintain continued compliance
Built on a big data frame work
On time safety reporting
Manage safety signals
Inbuilt signal/ risk management system
Delivers built-in, easy-to-use analytics
Insight into drug safety
IntelliVigil helps pharmaceutical and medical devices companies to identify bottlenecks in case processing process, address them early before they result in non-compliance.
Using IntelliVigil, biopharmaceutical organizations can automate and streamline their entire clinical development process through regulatory submission, post-approval trials, and pharmacovigilance
We can help to simplify processes across applications, reduce cycle times, and make in stream decisions while providing a higher level of traceability and compliance.
We are deeply committed for delivering process centric solutions for the most effective user experience with seamless workflow across all life sciences industry
Our end to end life sciences solution can provide the industry’s lowest total cost of ownership and can scale to the need of the largest and most complex studies across organization
IntelliVigil enables life sciences firms to aggressively detect and manage emerging safety risks to ensure patient safety, minimize costs and assure compliance.Schedule A Live Demo