Clinical Trials The effort and time consumed gathering data about the effects of a new drug on patients is enormous in Phase III and IV clinical trials. With current methods and systems resolving queries, alerting investigators to serious adverse events (SAE) or closing the trial after the last patient has visited (LPLV) are all hindered. AKAS provides the solution. The application and database required to gather and manage data are easily created and deployed across Intranets, Extranets or the Internet using the AKAS Builder and Server modules. Multiple layers of security can be applied to protect the sensitive data. Queries can be resolved dynamically using the monitoring feature, participants can be notified rapidly about SAE’s and the database which is updated in real time can be closed after LPLV within hours.