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VA Technical Reference Model v 24.4

Provation endoPRO iQ
Provation endoPRO iQ Technology

General InformationGeneral Information help

Technologies must be operated and maintained in accordance with Federal and Department security and privacy policies and guidelines. More information on the proper use of the TRM can be found on the TRM Proper Use Tab/Section.

Website: Go to site
Description: EndoPRO iQ is a comprehensive information management and image capture system that supports all stages of the endoscopy clinical workflow. This technology streamlines patient care and operation performance from patient arrival to patient discharge. This technology enables physicians and nursing staff to manage patient scheduling, archive procedure information, generate procedure gastrointestinal (GI) unit reports, and capture and annotate procedure images.

This technology can utilize a Microsoft Structured Query Language (SQL) Server database.

Note: Additional modules/components can be purchased for supplementary features.

Please note: Provation Software, Inc acquired the endoPRO software portfolio from PENTAX Medical in September of 2021; following the acquirement of the technology the company changed the name to Provation endoPRO iQ.
Technology/Standard Usage Requirements: Users must ensure their use of this technology/standard is consistent with VA policies and standards, including, but not limited to, VA Handbooks 6102 and 6500; VA Directives 6004, 6513, and 6517; and National Institute of Standards and Technology (NIST) standards, including Federal Information Processing Standards (FIPS). Users must ensure sensitive data is properly protected in compliance with all VA regulations. Prior to use of this technology, users should check with their supervisor, Information Security Officer (ISO), Facility Chief Information Officer (CIO), or local Office of Information and Technology (OI&T) representative to ensure that all actions are consistent with current VA policies and procedures prior to implementation.
Section 508 Information: This technology has not been assessed by the Section 508 Office. The Implementer of this technology has the responsibility to ensure the version deployed is 508-compliant. Section 508 compliance may be reviewed by the Section 508 Office and appropriate remedial action required if necessary. For additional information or assistance regarding Section 508, please contact the Section 508 Office at
Decision: View Decisions

Decision Source: TRM Mgmt Group
Decision Process: One-VA TRM v22.10
Decision Date: 10/11/2022 at 17:36:18 UTC
Introduced By: TRM Request
Vendor Name: Provation Medical
- The information contained on this page is accurate as of the Decision Date (10/11/2022 at 17:36:18 UTC).