Clinical Trials

Offload the Overload

InfoEd Clinical Trials brings order to the complex world of human studies.

InfoEd Clinical Trials links trials to related protocols, grants or contracts, publications, and patents. Accessible anytime from anyplace, InfoEd Clinical Trials reduces administrative burdens and workloads by consolidating information in a single location that facilitates collaboration between all the research personnel supporting your trial.

Principal Investigators and Researchers

  • Quickly locate the information you’re looking for
  • Helps to prioritize and reduce work loads
  • Easily and quickly support required approvals for faster study start-up and site activation
  • Links to all other project data – protocols, grants or contracts, publications, and patents
  • 360 degree trial management:
    • Trial design
    • Participant database
    • Document management
    • Collaborative communications
    • Financial tracking and reporting

Administrators and Coordinators

  • Simplifies tracking of multiple PI’s, trials, and participants
  • Immediately view any information across your trials
  • No redundant data entry
  • Communications are timely, and expertly documented
  • Documentation is version controlled, organized and easily updated
  • Compliance is easily facilitated on the front-end and quickly verified on the back-end
  • Security is role-based and flexible, yet easy to configure
  • History is recorded, documented and editable

InfoEd Clinical Trials Core Functions

Trial Design

  • Investigators can quickly build out the arms, visits, cycles, procedures, and billable events that make up a clinical trial protocol
  • All administrative and protocol details can be coded and tracked
  • Electronic case report forms can be developed using an intuitive tool that also supports the creation of libraries of questions – even entire forms – for reuse, accelerating the setup process for future trials

Recruitment

  • Participant database can interface with a variety of commercial and homegrown EMR systems
  • Easily match participants to trials, or conduct feasibility assessments to determine whether the clinical site has the population necessary to conduct a given trial
  • Track all aspects of an individual’s enrollment and trial participation from initial contact to completion or withdrawal

Document Management

  • Store all trial-related information, correspondence and documents directly within the trial record.
  • Provides a virtual regulatory binder that can be customized to support varying business needs and to maintain a wide variety of documentation for compliance with federal, state, local and institutional requirements

Reporting & Monitoring

  • Standard reports and ad hoc reporting tool provide views of trial data on demand, making it easy to monitor trial progress and quickly spot missing data elements
  • Clinical trial record includes a section for tracking monitoring visits, audits, and routine compliance reviews and their outcomes