NetRegulus Study

Study Administrator

Rapidly create and configure studies and effectively oversee the study's conduct.

  • Set up new studies and sites quickly and easily
  • Create study visit plans
  • Configure workflow and data processes to your own requirements
  • Track and monitor study and site tasks, milestones and documents
  • Create budgets and manage CRF & Attachment payment information
Study Data Manager

Facilitate all aspects of Subject enrollment and data collection. Provides access to all Subject-related data using the settings you configured within the Study Administrator module.

  • Enter study Subjects using study-specific enrollment CRFs
  • View the Subject’s progress in the study visit plan
  • Enter, verify, monitor, review and perform other tasks dictated by the study for the collection of CRFs and Attachments
  • Create Subject-level unscheduled visits
  • Create manual field, form and Attachment Queries and manage manual and automatically generated Queries
  • Use integrated reporting tools to access Subject, Visit, CRF, Attachment or Query records and to summarize and chart CRF data
Case Report Form Builder

Non-technical users can rapidly create CRFs that include integrity checks and can be used across one or more studies. CRFs may be mapped to new or existing data structures, including those designed specifically for tabular data.

  • Build CRFs quickly, with a wide selection of field types and formatting
  • Use a library of pre-configured field types
  • Create your own reusable fields and field groupings
  • Create intelligent data entry forms with built-in logic
  • Customize existing forms with company-specific graphics
  • Automatically enable sophisticated audit trail and form verification
Case Report Form Administrator

Manage your library of CRFs with a powerful search-reporting engine.

  • Update the underlying data structures for all of your CRF fields
  • Tailor specific rules for automatic field queries
  • Use Integrated Reporting Tools to create complex form queries or ‘Watchdog’ alerts
Adverse Events Manager

Manage adverse events, including initiation, triage, validation, medical review, submissions and closure. Query and mine data and conduct analyses of similar events. Adverse Events can also be launched directly from the Study Data Manger or the Complaints modules.

NetRegulus Technical Support