CLÆRITY® is easy-to-use web-based software for investigation and management of potential safety signals in adverse event data:
- Detect and investigate signals
- How do safety profiles of similar drugs compare?
- Manage and monitor signal investigation workflow
- Classify signals of interest
- Track and monitor selected signals over time
- Document actions and decisions
- Generate summary status and detailed signal history reports
CLÆRITY Benefits
- Signal investigation for multiple SRS databases, including: FDA AERS, FDA VAERS and Internal Company SRS Data
- Detect and investigate potential safety signals
- Manage and monitor signals over time
- Document and track outstanding actions
- Use complementary data mining technologies (PVmaps®, PRR, MGPS) for full coverage
- Flexible software licensing options to suit the specific safety information needs of both large and small pharmaceutical companies.
CLÆRITY-based service
- Ongoing surveillance, based on new releases of SRS data sources
- In-depth characterization of the safety profile of a drug or drug class
- "Clean" version of AERS data, including drug name normalization and mapping of obsolete MedDRA Terms
- Reference Event Database containing up-to-date literature references found for a specific drug and/or adverse event
