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Products

BioPharm Systems specializes in the following Oracle Health Sciences applications:

In order to provide organizations with cost-effective and sensible alternatives to traditional methods of implementing these clinical and safety applications, we have developed a series of innovative approaches, accelerators, and products. Years of experience packaged and delivered in just a matter of days or weeks. That is what BioPharm Accelerate is all about.

  • Accel-Account Manager: an innovative and easy-to-use clinical account management solution that allows managers of Oracle Clinical (OC), Remote Data Capture (RDC), and Thesaurus Management System (TMS) to create and maintain user accounts
  • Accel-Copy: a solution for copying, migrating and archiving Oracle Clinical studies and global libraries, as well as refreshing study patient data
  • Accel-Migrate: a cost-effective solution designed to help companies migrate to Argus Safety from a legacy pharmacovigilance system
  • Accel-NLV: two programs that streamline and enhance the collection of laboratory data in Oracle Clinical and Remote Data Capture (RDC)
  • Accel-Safety: a validation-ready version of Oracle's Argus Safety
  • Accel-Tracker: a pre-configured version of Empirica Topics, which is a powerful tool that helps companies track and manage information and activities that are related to potential drug safety and pharmacovigilance signals
  • ASCEND: a pre-configured and enhanced version of Oracle's Siebel Clinical Trial Management System (CTMS)
  • ASCEND-Migrate: a migration tool that transfers contacts, accounts, and addresses from your legacy investigator database to Siebel Clinical
  • Simple Forms: an affordable alternative to traditional electronic data capture (EDC) systems that can be used with Oracle Clinical
  • SOP Packages: procedural documentation that assists organizations with establishing process standards
  • Study Data Mapper: a web-based application that improves the operational efficiency of CDISC SDTM preparation, reporting standardization, management of clinical data standards, and conversion of legacy trials
  • Validation Packages: a comprehensive set of document and templates, ready for customization to meet regulatory and business needs

 

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