ARI Clinical Services

"ARI's" Emonitor is the leading provider of advanced data management solutions for clinical trials and drug safety, offering proven solutions in electronic data capture (EDC), data management, and adverse event reporting (AER) as either an integrated solution or as stand-alone applications. We offer you the leading products in data capture, data management, and safety as an integrated solution.

Emonitor is a comprehensive HIPAA, 21 CFR Part 11 compliant SAS®-based system for managing clinical trials including CRF tracking, data entry, and review. The simple interface allows you to set up your clinical studies in days. Emonitor

leverage the power of the Internet for rapid data capture and processing, no special hardware or software installations required at the sites, reduces the overall trial cost significantly, reduces human error dramatically and saves time.

Emonitor is platform independent, uses Cutting Edge Java Technology supports practically any popular database (Oracle/MS SQL and others), highly configurable, secured (SSL) with digital Signature support, fast and efficient, easy to use and dynamic XML forms are saved in database. It allows instant viewing of data, automatic audit trail for every steps, real time edit check engine and instant feedback to users. Automatic query generation, manual DCF creation, easy query tracking and review by admin users. Automatic data locking for forms, individual answers and easy signing of data after review.

Emonitor's advanced data management system is one stop shopping for your clinical trial need with integrated document processing, full support for international ( double-byte) character sets concurrent usage in multiple languages provides capabilities for multi-national trials as well as a single database support for international operations. It provides user interface and work flow capabilities for both endpoint-driven protocols as well open ended surveillance studies and registries.

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