CONTEXT:
In a clinical trial for a cardiovascular drug, our client faced challenges in detecting rare adverse events due to the sheer volume and complexity of safety data. Identifying meaningful patterns required a more efficient and reliable approach.

RESOLUTION:
Our data analysts leveraged SAS procedures such as PROC SQL and PROC FREQ to conduct detailed safety data analyses and uncover trends in adverse events. To streamline the process, custom SAS macros were developed, enabling automation of routine safety analyses. This not only increased efficiency but also improved the accuracy and consistency of safety monitoring.

RESULT:
The solution adhered to good programming practices, reducing the risk of errors and ensuring high data quality. As a result, potential safety concerns were identified more promptly, enabling the client to make timely and informed risk assessments throughout the drug development process.