With Appian, the high demands of intake and detection, safety information management, and adverse events reporting can be organized and managed within a unified platform.
A large, multinational pharmaceutical company with 100,000+ employees ran on a dangerously inefficient legacy paper-based process that was dangerously inefficient. With Appian low-code automation, they were able to automate key steps to concurrently speed processes and reduce errors, along with unifying data across multiple systems.
See why life sciences organizations trust Appian for pharmacovigilance to automate the processing of adverse event signals by effectively logging and investigating drug safety issues.
See why organizations require an innovative pharmacovigilance solution for regulatory reporting, managing massive amounts of data, and more.