Drug safety and pharmacovigilance 

Simplifying processes in case intake, triage, and reporting with AI-enabled automation. Accelerating drug safety monitoring and increasing its effectiveness while reducing the need for manual effort.

Seamlessly integrating safety data from various sources. Helping organizations establish comprehensive monitoring and analysis, facilitating better decision-making in pharmacovigilance.

Leveraging ML techniques to improve risk detection. Assisting companies in switching to the proactive mode of anticipating safety concerns and taking steps to intervene in a timely manner.

Enhancing pharmacovigilance procedures to help companies meet the evolving regulations. Helping Life Sciences companies increase submission efficiency, accuracy, and traceability.

Enabling real-time tracking and analysis of adverse events. Enabling organizations to enhance responsiveness to potential drug safety issues and implement timely interventions.

Using AI-powered screening to reduce inefficiencies in literature monitoring. Aiding Life Sciences companies in reducing errors, increasing precision, and quickening the detection of adverse events.

Managing vast volumes of adverse event data from diverse sources – such as EHRs, social media, medical literature, and global databases – is extremely challenging. By integrating AI technologies into workflows, organizations can significantly enhance their data management. We help them use the right ML architectures to enhance both the accuracy and timeliness of safety signal detection. 

Multiple pharmacovigilance workflows can be transformed by cleverly implementing custom, advanced tech.  We build bespoke solutions for life science companies looking to enhance data collection, data safeguarding, case reporting, inter-department collaboration, safety signal identification, and more. 

When routine pharmacovigilance processes – intake, triage, and reporting – are automated, the staff can focus on more value-added activities, like signal detection and risk analysis. We assist organizations in incorporating automation, helping them drastically reduce errors, inefficiencies, and operational costs of manual procedures. 

We understand the complexities of navigating global regulatory requirements for Life Sciences companies. We help them utilize advanced tech and build custom platforms that enable them to streamline pharmacovigilance processes while ensuring seamless adherence to critical regulations such as FDA, EMA, and PMDA.