Adverse Event Reporting

Adverse Event Reporting (AER) is a critical process in healthcare, enabling healthcare organizations to identify and report adverse events related to medical devices, pharmaceuticals, and other healthcare products. While AER is a necessary process, it can be time-consuming and resource-intensive. However, with Decision Engines’ prebuilt connector bots, healthcare organizations can now automate their Adverse Event Reporting process, saving time and resources while ensuring compliance with regulations.

Decision Engines’ prebuilt connector bots are designed to integrate with various data sources, including electronic medical records, patient safety reports, and other healthcare data sources. These bots use natural language processing and machine learning algorithms to identify and extract relevant information related to adverse events, such as patient demographics, medical histories, symptoms, and treatment information.

Once the information is extracted, the bots use predefined business rules to classify the adverse event based on severity and other factors. The bots can also automatically generate reports and notify the appropriate stakeholders, including regulatory authorities, healthcare providers, and patients.

The benefits of using Decision Engines’ prebuilt connector bots for Adverse Event Reporting are significant. By automating the process, healthcare organizations can reduce the risk of errors and improve the accuracy and completeness of adverse event reports. This, in turn, can help to improve patient safety and outcomes.

Moreover, automating AER with Decision Engines’ prebuilt connector bots can save healthcare organizations time and resources by eliminating manual data entry and report generation. This can free up healthcare professionals to focus on providing patient care and other critical tasks.

Use Case

A use case for healthcare industry to utilize Decision Engines’ prebuilt connector bots for AER could be for medical device manufacturers. For example, a medical device manufacturer may have thousands of devices in use across the country. In the event of an adverse event related to one of their devices, the manufacturer would need to quickly identify the affected patients, determine the severity of the adverse event, and report the incident to regulatory authorities.

With Decision Engines’ prebuilt connector bots, the manufacturer can automate this process, quickly identifying the relevant patient data, classifying the event based on severity, and generating reports for regulatory authorities. This can help the manufacturer to meet regulatory requirements and ensure patient safety, all while saving time and resources.

Why Choose Decision Engines

Decision Engines’ prebuilt connector bots provide healthcare organizations with a powerful tool to automate their Adverse Event Reporting process. By leveraging natural language processing and machine learning algorithms, healthcare organizations can improve the accuracy and completeness of adverse event reports while saving time and resources. With its potential to improve patient safety and outcomes, Decision Engines’ prebuilt connector bots are a valuable investment for any healthcare organization.

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