Electronic Health Record System

Location: Tennessee
Posted: May 12, 2026
Due: Jun 15, 2026
Agency: State Government of Tennessee
Type of Government: State & Local
Category:
  • 70 - General Purpose Information Technology Equipment (including software).
  • D - Automatic Data Processing and Telecommunication Services
  • R - Professional, Administrative and Management Support Services
Solicitation No: RFI 33901-00393
Publication URL: To access bid details, please log in.
Document ID & Hyperlink: RFI 33901-00393
Event Start - Response Due: 05/11/2026

06/15/2026
Event Name: Electronic Health Record System
Last Updated:

Attachment Preview

STATE OF TENNESSEE
DEPARTMENT OF MENTAL HEALTH AND SUBSTANCE ABUSE SERVICES
REQUEST FOR INFORMATION
FOR
ELECTRONIC HEALTH RECORD SYSTEM
RFI # 33901-00393
MAY 11, 2026
1. STATEMENT OF PURPOSE:
The State of Tennessee, Department of Mental Health and Substance Abuse Services
(TDMHSAS) issues this Request for Information (“RFI”) for the purpose of reviewing options
available for an Electronic Health Record (“EHR”) system. We appreciate your input and
participation in this process.
2. BACKGROUND:
The Tennessee Department of Mental Health and Substance Abuse Services operates four (4)
Regional Mental Health Institutes (RMHIs) that provide inpatient psychiatric care and treatment
for individuals across the state. These facilities are located in Chattanooga, Nashville, Bolivar,
and Memphis, and collectively serve a patient population with complex behavioral health needs.
Across these facilities, TDMHSAS supports approximately six hundred (600) inpatient beds. The
current clinical and administrative operations are supported by an estimated two thousand (2,000)
named system users, with approximately four hundred (400) concurrent users at peak utilization.
TDMHSAS is seeking information from qualified vendors regarding EHR) systems and related
solutions that can support and enhance inpatient behavioral health operations. The Department is
particularly interested in modern, scalable platforms that provide workflow optimization, advanced
clinical tools, robust reporting and analytics, interoperability and integration capabilities, artificial
intelligence (AI)-enabled functionality, and strong data privacy and security controls.
3. COMMUNICATIONS:
3.1. Please submit your response to this RFI via email to:
Mary Lee, Director of Contracts/Senior Associate Counsel
Tennessee Department of Mental Health and Substance Abuse Services
Mary.Lee@tn.gov
3.2. Please feel free to contact the Department of Mental Health and Substance Abuse Services
with any questions regarding this RFI. The main point of contact will be:
1
Mary Lee, Director of Contracts/Senior Associate Counsel
Tennessee Department of Mental Health and Substance Abuse Services
Mary.Lee@tn.gov
(615) 587-1557
3.3. Please reference RFI # 33901-00393 with all communications to this RFI.
4. RFI SCHEDULE OF EVENTS:
EVENT
1. RFI Issued
2. RFI Response Deadline
TIME
DATE
(Central Time (all dates are State
Zone)
business days)
May 11, 2026
4:00 p.m.
June 15, 2026
5. GENERAL INFORMATION:
5.1. Please note that responding to this RFI is not a prerequisite for responding to any future
solicitations related to this project and a response to this RFI will not create any contract
rights. Responses to this RFI will become property of the State.
5.2. The information gathered during this RFI is part of an ongoing procurement. In order to
prevent an unfair advantage among potential respondents, the RFI responses will not be
available until after the completion of evaluation of any responses, proposals, or bids
resulting from a Request for Qualifications, Request for Proposals, Invitation to Bid or other
procurement method. In the event that the state chooses not to go further in the
procurement process and responses are never evaluated, the responses to the
procurement including the responses to the RFI, will be considered confidential by the
State.
5.3. The State will not pay for any costs associated with responding to this RFI.
6. INFORMATIONAL FORMS:
The State is requesting the following information from all interested parties. Please fill out the
following forms:
2
RFI #33901-00393
TECHNICAL INFORMATIONAL FORM
1. RESPONDENT LEGAL ENTITY NAME:
2. RESPONDENT CONTACT PERSON:
Name, Title:
Address:
Phone Number:
Email:
3. Describe your organization, ownership structure, financial stability, years providing behavioral
health EHR solutions, and any mergers or acquisitions within the past five (5) years.
4. Describe your experience supporting state-operated or government-operated inpatient
psychiatric hospitals, including the number of facilities currently served, approximate bed
counts, length of time organizations have been live on your platform, and at least three public-
sector psychiatric hospital references.
5. Describe lessons learned, implementation challenges, and operational outcomes from
supporting multi-facility state-operated psychiatric hospitals operating under centralized
governance.
6. Describe your experience working within government procurement, cybersecurity, audit, public
records, and regulatory compliance environments.
7. Describe how your platform supports core psychiatric inpatient workflows, including
admissions, transfers, discharges (ADT), psychiatric evaluations, multidisciplinary treatment
planning, and discharge planning.
8. Describe how your platform supports seclusion, restraint, suicide precautions, violence risk
management, observation levels, escalation workflows, alerts, and regulatory compliance
tracking.
9. Describe how your platform supports forensic and competency-to-stand-trial patient
populations, including legal status management, court-related workflows, and patient tracking
10. Describe treatment planning capabilities, including workflow design, version control,
multidisciplinary collaboration, and whether treatment plans can be maintained as a single
longitudinal record versus multiple fragmented components (e.g., initial plan, reviews, master
plans, updates).
11. Describe how diagnoses, problem lists, and care plans are managed over time, including
historical tracking, inactive diagnoses, versioning, and lifecycle management across the patient
record.
12. Describe psychiatric nursing workflows, including shift handoffs, rounding, observation
documentation, safety checks, and behavioral/incident event capture.
13. Describe support for unit operations, including census management, bed management, staffing
visibility, and operational throughput.
14. Describe how your platform supports hospital-grade medication workflows, including
computerized provider order entry (CPOE), electronic medication administration records
(eMAR), medication reconciliation, psychotropic workflows, and PRN medication management.
15. Describe your platform’s closed-loop medication management capabilities, including barcode
medication administration, medication verification, and patient safety controls.
16. Describe medication-related alerts, warnings, hard stops, adverse reaction documentation,
refusal documentation, and medication error tracking.
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17. Describe how your platform integrates with automated medication dispensing systems (e.g.,
Pyxis or similar solutions). Include support for real-time medication order interfacing, cabinet
inventory management, user authentication, controlled substance workflows, discrepancy
handling, override tracking, and reconciliation processes. Please also describe your integration
approach, supported vendors, data flow, and any dependencies on third-party systems or
middleware.
18. Describe whether your platform includes a fully integrated pharmacy management module. If
yes, describe capabilities including medication formulary management, order verification,
dispensing workflows, compounding support, inventory management, controlled substance
tracking, and pharmacist clinical review workflows.
19. Describe the level of local configuration and control available to a single customer/entity (e.g.,
Tennessee) to implement workflow, documentation, form, or compliance changes without
requiring network-wide consensus or vendor-wide standard changes. Include examples related
to state law changes, The Joint Commission findings, and internal workflow improvement
requests. Clearly identify what changes can be performed locally versus those requiring vendor
development, governance approval, or global release cycles.
20. Describe governance models used by organizations operating multiple hospitals on a shared
platform, including change control, enterprise standardization, configuration ownership, and
facility-specific workflow management.
21. Describe compliance with Centers for Medicare & Medicaid Services standards, The Joint
Commission requirements, Tennessee regulations, and patient rights documentation.
22. Describe support for 42 CFR Part 2 compliance, including data segmentation, consent
management, and access restrictions.
23. Describe record retention capabilities, including policy flexibility, configurable retention
schedules, historical record management, archival workflows, and support for state-specific
retention requirements. Include whether retention can be managed more flexibly than an “all-
or-nothing” retention model.
24. Describe your platform’s interoperability capabilities, including support for HL7, FHIR, CDA,
APIs, and integration with ADT systems, laboratory systems, pharmacy systems, health
information exchanges, and third-party clinical applications.
25. Describe transition-of-care capabilities, including discharge summary exchange, coordination
with community providers, emergency departments, courts, forensic agencies, and correctional
systems.
26. Describe your current third-party integration ecosystem and provide a list of external
vendors/systems commonly integrated with your EHR across your client network.
27. Describe enterprise reporting, analytics governance, self-service reporting, and statewide
reporting capabilities across multi-facility public-sector healthcare organizations.
28. Describe your organization’s analytics and reporting capabilities, including native dashboards,
ad hoc reporting tools, and executive/operational dashboards. Please specify whether
dashboards are included in the base product or offered as add-ons, what data domains are
supported (e.g., clinical, operational, financial), how frequently data is refreshed (e.g., real-
time, near real-time, batch), and whether customers can build and maintain custom
dashboards without vendor development or professional services.
29. Describe the technical documentation available to support enterprise analytics, including data
dictionaries, schema documentation, data lineage, and ETL documentation.
30. Does your EHR include an integrated billing or revenue cycle module? If yes, describe
capabilities including registration, eligibility/benefits, authorizations, charge capture, coding
support, claims generation, remittance/ERA posting, denial management, patient statements,
4
and collections. If not native, identify commonly integrated billing vendors and how integrations
function.
31. Describe your support for claims processing, payer connectivity, and clearinghouse
integrations. Identify which clearinghouses are commonly supported and describe data flow,
timing, reconciliation, and exception handling.
32. Describe your platform’s security architecture, including encryption standards, role-based
access controls, audit logging, breach detection, incident response, and downtime workflows.
33. Describe the technical architecture of the solution, including hardware platform, operating
systems, database platform, application servers, web servers, middleware, infrastructure
dependencies, and supported deployment models. Please indicate whether vendor-hosted,
cloud-hosted, on-premise, or hybrid deployment options are available.
34. Describe your hosting, infrastructure, uptime commitments, disaster recovery, business
continuity planning, and service-level commitments supporting 24/7 inpatient hospital
operations.
35. Over the next three (3) years, are there any planned upgrades, platform changes, module
retirements, architectural changes, or product roadmap items that could materially impact
current functionality, integrations, performance, supportability, training, or downtime? If yes,
please describe planned changes, timing, customer impact, and mitigation approach.
36. Describe compliance with accessibility standards, including WCAG 2.1 AA, Section 508, VPAT
availability, accessibility testing, and usability validation practices.
37. Describe how accessibility is incorporated into clinical workflows, release governance, usability
testing, product design, and continuous user experience improvements.
38. Describe your implementation methodology for a multi-facility state-operated healthcare
environment, including timeline, sequencing, governance, and risk management.
39. Describe your data migration methodology, including scope, validation, historical conversion,
and legacy system transition support.
40. Describe your training methodology, including role-based training, super-user programs,
adoption strategies, and post-go-live support.
41. Based on organizations of similar size, census, and user complexity, what IT support staffing
model do you recommend for successful long-term support of your platform? Please include
recommended staffing roles, staffing ratios, operational responsibilities, and support structure
considerations.
COST INFORMATIONAL FORM
1. Describe pricing model.
2. Identify cost components (licensing, implementation, interfaces, training, support and provide
ballpark estimates.
3. Identify optional/modules/add-ons.
4. Describe post-go-live costs.
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This is the opportunity summary page. It provides an overview of this opportunity and a preview of the attached documentation.
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