CONTEXT:
A healthcare client conducting global clinical trials needed to monitor and manage adverse drug reactions across multiple countries. The primary challenge was detecting patterns in large-scale safety data submitted by hospitals, research centers, and regulatory portals.

RESOLUTION:
Our SAS experts developed a dynamic framework for real-time adverse event reporting. By leveraging PROC SQL, PROC REPORT, and advanced SAS Macros, the system quickly flagged serious adverse events and produced standardized reports for global regulatory agencies.

RESULT:
This enhanced reporting mechanism enabled faster detection and resolution of safety issues, improving both patient safety and regulatory compliance. Communication with authorities was streamlined, fostering greater transparency and trust in the drug’s safety profile.