Argus J™ fully integrates Japan into the world-wide business process, enabling global pharmaceutical companies to realize significant productivity benefits. Argus J™ is the comprehensive solution to manage all Japanese reporting requirements.

Single Global Database

Argus J™ integrates seamlessly with the Argus Safety™, providing a single global database with unified workflow for management of world-wide drug safety information. Pharmaceutical companies realize productivity gains by eliminating double data processing efforts. Argus J’s truly global configuration also improves manageability and simplifies system maintenance for administrators.

World-wide Regulatory Reporting

Argus J™ integrates seamlessly with Argus Interchange™, meeting worldwide requirements for electronic submissions. Spontaneous, Periodic, and Clinical Expedited Reports can be easily transmitted to the PMDA.

Advanced Multi-Language Tools

Argus J™ adds Japanese local fields to support Japanese requirements. Argus J™ also supports Japanese translated code lists and contains a PMDA screen for Japan-specific case information. Translation support tools allow coded values to be automatically translated from Japanese to English, and vice versa. In addition, Argus J™ includes MedDRA and MedDRA J browsers and supports the Japanese Drug Dictionary.