The FDA has launched a new adverse event reporting system that will consolidate several systems it has for reporting different types of adverse events, the agency announced Wednesday. The new system, ...

FDA replaces seven fragmented adverse event databases with AEMS, enabling real-time safety signal access for pharmaceutical manufacturers and researchers. On March 11, the FDA launched a unified ...

Colorado Springs, Colo., July 19, 2021 (GLOBE NEWSWIRE) -- Bold Group, an industry-leading purveyor of event monitoring, business automation, and cybersecurity solutions for the electronic security ...

The auditing and monitoring process is critical to a compliance program’s success, in that it provides ongoing assessment of processes, procedures, and potential escalation of risk. Designed as an ...