ClinicalPURSUIT is a web based software that can monitor adverse events, complications and help you to manage patient safety. Your patient registry initiative should require a Patient Safety and Monitoring Plan (PSMP). A PSMP describes how the study investigators will oversee patient safety and how adverse events will be graded, characterized, and reported. The plan should be tailored to fit each study.
A simple plan may be adequate for a minimal risk study; a more detailed plan will be required for above minimal risk studies. Let us show you how our software can be easily tailored to fit your business rules and drivers. Your patient safety and SAE monitoring should leverage web-based software that is not only tailored but effortless to navigate.
Patient Safety, A National Priority
While this has always been at the heart of our software development its never been more significant than in this moment. To evaluate interventions for reducing medical errors and adverse events, effective methods for detecting such events are required. It's important that your organization considers a framework for error monitoring and detection. A system that can automatically notify your team of each occurrence.
With our patient registry software system you can record, track and monitor serious adverse events using free-text clinical narratives, coded data, pre-formatted FDA specific CRF's....or a combination of techniques. With our software you can easily track and monitor multiple SAE potential sources.
Private, Secure, HIPPAA Compliant
There have been advances in these systems with regards to HIPAA compliance, security and safety checking. These systems include email notifications to sponsors and medical affairs/regulatory groups - the instant a serious adverse event is recorded in a registry system that can greatly facilitate your ability to monitor adverse events and promote patient safety research.