SCIAN: EDCPRO & SAEPRO for Clinical Trials

By: Scian  09-12-2011
Keywords: Access Control, data management, Data Entry

SCIAN: EDCPRO & SAEPRO for Clinical Trials

EDCPRO is a powerful and effective Web-based clinical data management system that incorporates SciAn's 15 years of EDC knowledge and experience in managing oncology clinical trials. Founded on our therapeutic area expertise, theintuitive user interface helps Study Coordinators and Monitors complete their data management tasks with ease, efficiency and minimum administrative overhead.

EDCPRO guides Study Coordinators and Monitors towards consistent data collection and protocol interpretation.  In addition,  the system was designed with a comprehensive suite of data management tools to support the work of Medical Monitors, Database Managers (tools for coding, SAE reconciliation, preparation of database for DSMBs, interim and final analyses, etc).

Key Features of EDCpro:

  • Intuitive, user-friendly interface
  • FDA 21 CFR Part 11 compliant
  • Comprehensive Help System
  • Proprietary "Guided Data Entry"™ system
  • Training manuals
  • User qualification module (on-line Quiz)
  • User registration and access control management module
  • Customizable workflow to match clients' business practices and SOPs
  • On-line case histories - plots
  • Status reports
  • Excel database export
  • Data import and export using CDISC ODM compliant XML format.

Keywords: Access Control, Access Control Management, Clinical Data, Clinical Data Management, Clinical Trials, Data Entry, Data Import And Export, data management, Data Management System, Database Export, Excel Database, Management Tasks, status reports, Study Coordinators,

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