CLÆRITY^® is easy-to-use web-based software for investigation and management of potential safety signals in adverse event data:

• Detect and investigate signals
  • What are the significant signals for a drug, class, or group?
  • Is the signal strength changing over time?
  • Is the signal part of a bystander effect or a drug-drug interaction?
  • 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 of interest over time
• Document and track outstanding actions
• Use complementary data mining technologies (PVmaps^®, PRR, MGPS) for full coverage

CLÆRITY Products and Services

• CLÆRITY License: ProSanos offers 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 underlying SRS data sources
  • In-depth, historical 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

To see real case studies using CLÆRITY, visit our PVmap of the Week