Responses Due By

2024-05-03 23:59:59 US/Eastern Time

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Digital Front Door Plus

Project Description

Problem Statement. The Military Health System (MHS) is at an inflection point, reflecting risks and challenges that are both unique to military medicine, and reflect overall health care challenges in the United States (e.g., increased utilization of high-cost services; shortages of nurses, technicians, and physicians; rapid and costly changes in technology; access challenges for individuals living in remote and medically underserved communities). 


The MHS cannot sustain the readiness of the medical force in the present operating model. The accelerating shift in healthcare to digitalization, patient-centeredness and hyper-specialization requires the Defense Health Agency (DHA) to adapt or see a reduced readiness of the medical force, deteriorating retention of medical staff, and reductions in direct care capability and capacity that will be almost impossible to reverse. 


Priorities. A new model for delivering care and a technology-enabled framework for adapting and evolving is required. The new model and framework will center on several priorities that take advantage of available and emerging technologies and allow new technologies to be added within the military healthcare ecosystem. These priorities are:


   Human centered. The MHS is woefully behind the patient-centered technology offerings of most large health plans and healthcare delivery systems. Tools are needed that allow its 9.5 million beneficiaries to better manage their own health and wellness requirements. The desired solution is a “digital front door” that successfully integrates with or replaces our current architecture, is data centric and platform agnostic, and is capable of rapid adaptation. The expectation is for beneficiaries to self-schedule with virtual, asynchronous, and in person visit options; use secure messaging; participate in patient intake; utilize satisfaction surveys; seek referrals; engage with live chats; find providers; and access patient education, medical records and lab results.


   A Competitive Health Ecosystem. Technologies that military health workers have access to must match or exceed what civilian health workers enjoy today. A competitive Health Ecosystem removes administrative, cognitive, and repetitive burdens from the workforce. The initial focus is on the outpatient setting and begins with primary care and behavioral health. Proceeding from an outpatient to inpatient setting, the health ecosystem will adapt currently available solutions.

 

DHA will prioritize its investment strategy to deliver the capabilities the DoD needs today and in the near future; rapidly partnering with leaders in healthcare technology and services; incorporating TRICARE contractors and network providers in solutions; and better using commercial tools available now to improve both patient and provider experiences.  


Desired Capabilities. DHA seeks commercial, platform agnostic solutions to support a patient experience that is frictionless for its beneficiaries; ensure patient interactions and data are collected in the MHS Information Portal (MIP); enable enterprise-managed multipurpose mobile devices, provider applications, digital assistants, and wearables that serve as the foundation to grow future initiatives; anticipate advances in the health sciences (precision medicine, pharmacovigilance, bio-surveillance).


DHA is seeking to continue to expand its suite of tools based on private sector advancements that assist in the transformation of patient care. The focus will be organized across three lines of effort (LOEs).


   (LOE) 1: Patient Experience – Changing the Care Model for Healthcare. DHA seeks a commercial solution(s) that enables the following priorities: frictionless access to care and services for beneficiaries; seamless integration with the existing Electronic Health Record; and complete interoperability with wearables and devices. 


A frictionless experience means that patients can securely access the full suite of health services with a single-sign-on, facilitated by machine learning and chatbots, that provides a longitudinal health record (medical history, medications, test results, reminders), connects patients to wellness and self-care packages, and/or assists patients in virtual, in-person or asynchronous visits within the Direct Care System or Private Sector Care. User interfaces are designed for mobile devices (phones, tablets, augmented/virtual reality), intuitive and require minimal customer support. 


Interoperability includes compatibility with enterprise or personally owned peripherals, wearables or medical devices.


Successful commercial solutions that focus on changing the care model will also offer access to recognized academic or thought leaders in healthcare systems, healthcare economics, health services research, wellbeing, public health and life sciences. Changing the value equations requires moving from a transactional, systems-based model to human centered model while maintaining quality and safety and retaining fiscal responsibility. The new model will place the business and mechanical aspects of healthcare in the background, while recentering on MHS patients as human beings and returning joy to the MHS workforce, reminding them why they entered healthcare in the first place.

  

   LOE 2: Provider Supported Technology in the Health Ecosystem. This effort will remove administrative, cognitive, and repetitive burdens from the workforce. The Health Ecosystem includes provider applications such as digital assistants that use generative AI to recognize speech and assist with workflows.


Over time, the Health Ecosystem will include applications for scheduling, virtual nursing, preventing alert fatigue, chart search, telemetry, remote patient monitoring and hospital command centers.

 

   LOE 3: Data Management Support - Foundation for Future Initiatives. This LOE is based on the intelligent and actionable use of data contained in the MHS Information Portal (MIP). The MIP consists of a logic layer (API Gateway, Data Exchange, File Transfer) that supports MOVEi, FHIR, JSON and HL7. The data layer (common data model, enterprise data, warehouse, structured data storage and enterprise data lake) support OMOP, SGL, S3 and Redshift. The MIP operates as the central integrated data broker and service provider for all healthcare operations. 


Commercial solutions build upon the MIP and will allow users at all levels of the MHS to access, manipulate, and present patient-specific and enterprise-wide health information for making policy, management, and resource allocation decisions. 


Background Information 

These LOEs may be executed by a single vendor bringing a comprehensive solution or by multiple vendors working in a teaming arrangement and demonstrating interoperability. 


Prototypes will be implemented through the DHA Accelerator, whose purpose is to identify, test and implement emerging solutions in ways that adapt our healthcare delivery model. The Accelerator operates across five MTFs serving a beneficiary population of approximately 260,000. The Accelerator will validate solutions at the five Military Treatments Facilities and prepare those solutions for enterprise-wide adoption. Minimally viable offerings from LOE 1 will be implemented at those five sites in six to twelve months from acceptance. 


Multiple agreement awards are anticipated, and a single company is not expected to provide a solution that covers all solution areas. Preference may be given to product mixes that include solutions with evidence of similar deployments. The DoD may facilitate teaming arrangements among submissions offering complimentary capabilities to achieve desired effect. Companies are also welcome to present their own teaming arrangements in their solution briefs. If technology solutions are proprietary, performing companies will be expected to establish business to business safeguards that permit information sharing amongst teaming members in pursuit of solutions. Academic research proposals are not desired. 


Successful prototypes will need network accreditation to ensure full functionality and deployment on DoD systems. Existing authority to operate (ATO) or certification as a system of record are a plus. Vendors must possess or be able to obtain necessary accreditations to deploy/operate their solutions in Defense Information Systems Agency (DISA) Impact Level 6 (IL6) environments.


*Note to offerors: It is anticipated human subjects research may be required in performance of any subsequent agreement(s). Therefore, offerors should be aware that compliance with 32 CFR 219, DoDI 3216.02 will be mandatory, as applicable.

Eligibility Requirements

Awarding Instrument

This Area of Interest solicitation will be awarded in accordance with the Commercial Solutions Opening (CSO) process detailed within HQ0845-20-S-C001 (DIU CSO), posted to SAM.gov on 13 Jan 2020, updated 02 Oct 2023. This document can be found at: https://sam.gov/opp/e74c907a9220429d9ea995a4e9a2ede6/view

FAQs

Q1: Can a for-profit company submit a response with a Government organization as a partner?


A1: Given the information provided in the question, we cannot make a determination regarding eligibility. We encourage you to apply and eligibility will be evaluated during Phase 1 of the CSO process.


Q2: What are the parameters for what businesses are eligible to submit? Are large business eligible to apply.


A2:Yes, large businesses are eligible to apply. Please refer to 10 USC 4022(d)(1)


Q3: Is there any information available as to the funding available for this solicitation?


A3: This information is not eligible for disclosure at this time.


Q4:If we are writing a paper on all three LOEs is it 5 pages per LOE?


A4: See Q&A #9.


Q5: Can we apply to only LOE 1 and LOE2 with a narrowly focused scope? Do we need to team up with other companies to submit a more comprehensive solution?


A5: We recommend submitting a solution brief(s) for the Government’s review and evaluation. Teaming recommendations are addressed in the Area of interest statement.


Q6: Does DIU anticipate selecting a vendor to prototype LOEs 2 and 3 in addition to LOE 1? If yes, will those prototypes be implemented at five sites in 6-12 months from acceptance as well?


A6: These LOEs may be executed by a single vendor bringing a comprehensive solution or by multiple vendors working in a teaming arrangement and demonstrating interoperability. Multiple agreement awards are anticipated, and a single company is not expected to provide a solution that covers all solution areas. 


Q7: Typically, IL6 is reserved for NSA, Defense Intelligence Agency, etc. Of note, the rest of the health tech at DHA/MHS is being implemented at an IL4 level and IL5 in some instances.So please explain why we need to possess or be able to obtain the necessary accreditations to deploy/operate in DISA Impact Level 6 (IL6) environments.


A7: Vendors must possess or be able to obtain necessary accreditations to deploy/operate their solutions in Defense Information Systems Agency (DISA) Impact Level 6 (IL6) environments. Vendors that do not possess, or minimally able to demonstrate the ability to obtain necessary accreditations will likely be removed from consideration.


Q8: Are EU based private companies eligible to apply?


A8: Given the information provided in the question, we cannot make a determination regarding eligibility. We encourage you to apply and eligibility will be evaluated during Phase 1 of the CSO process.


Q9: I want to verify that it is ok to submit two separate briefs, which each distinctly address each LOE with different products and services. Please confirm that we will not be disqualified for submitting two separate 5 page briefs, addressing LOE 2 and LOE 3.


A9: A single offeror may submit more than one solution brief as long as the proposed is not duplicative. 


Q10: Do you need a budget at this stage?


A10: No. Please refer to our CSO for explicit submission details and instructions. 


Q11: Do you want to see a research strategy or will a milestone list be sufficient at this stage?


A11: Per the AOI, DHA seeks a commercial, platform agnostic solutions to support a patient experience for its beneficiaries; ensure patient interactions and data are collected in the MHS Information Portal (MIP); enable enterprise-managed multipurpose mobile devices, provider applications, digital assistants, and wearables that serve as the foundation to grow future initiatives; anticipate advances in the health sciences (precision medicine, pharmacovigilance, bio-surveillance).


Q12: Can Canadians submit a solution to the following opportunity?


A12: Given the information provided in the question, we cannot make a determination regarding eligibility. We encourage you to apply and eligibility will be evaluated during Phase 1 of the CSO process.


Q13: We recognize the deadline is approaching and are wondering, is it possible to speak to a member of your team?


A13: Not at this time. We encourage you to apply and your solution will be evaluated during Phase 1 of the CSO process. If invited to Phase 2 your questions will be answered.


Q14: Currently, there is a 22-month delay on new FCLs after the DD-254 is submitted. What is the anticipated timeframe for the IL5 or IL6 requirements for the various LOEs? Will companies who need to initiate FCL at award be considered?


A14: At this time the Government cannot approximate the timeframe for IL5 or IL6 requirements. We encourage you to apply and consider Q&A #7. Companies who need to initiate FCL at award will be considered.


Q15: Given our European roots, but with a fresh US subsidiary (no commercial activity yet), should we apply through our US arm or would we still be seen as foreign-owned? If we apply solo and advance beyond the Solution Brief Phase, could we team up with others later? Or is partnering upfront the move? What's the timeline for getting compliant with DISA Impact Level 6 accreditations to deploy/operate in Defense Information Systems Agency (DISA) environments?


A15: Please see Q&A #8. It is advised that US subsidiaries apply as the solution offeror. We encourage you to submit an end to end solution for each LOE that includes teaming arrangement possibilities. However, teaming arrangements may transpire past initial solution offer at the discretion of the Government. Please see Q&A #14.


Q16: Can you please confirm that the deadline has been updated to May 3rd at midnight?


A16: The deadline to apply has been revised to 23:59:59 EST on 3 May 2024. 


Q17: Is it ok to include a link to a video(s) in our solicitation response? Will reviewers watch them? Are images better?


A17: Solution Briefs should not exceed five (5) written pages using 12-point font or, alternatively Solutions Briefs may take the form of briefing slides which should not exceed fifteen (15). A link to a video may be provided within the solution brief to the extent it is not unnecessarily elaborate. 


Q18: We want to apply with the focus on a better patient and provider experience in LOE 1 and LOE2. We will only cover medical imaging. Can we still apply? Do we need to team up with other companies to submit a more comprehensive solution?


A18: We encourage you to submit an end to end solution for each LOE that includes teaming arrangement possibilities.
















Before You Submit

What we recommend you include when you submit a solution brief.

When you submit to a DIU solicitation, we'll ask you to include a solution brief. Here's some guidance about what that entails.

Potential Follow-On Production Contract for Prototype Other Transaction Agreements

Companies are advised that any Prototype Other Transaction (OT) agreement awarded in response to this solicitation may result in the direct award of a follow-on production contract or agreement without the use of further competitive procedures. Follow-on production activities will result from successful prototype completion.

The follow-on production contract or agreement will be available for use by one or more organizations within the Department of Defense. As a result, the magnitude of the follow-on production contract or agreement could be significantly larger than that of the Prototype OT agreement. All Prototype OT agreements will include the following statement relative to the potential for follow-on production: “In accordance with 10 U.S.C. § 4022(f), and upon a determination that the prototype project for this transaction has successfully been completed, this competitively awarded Prototype OT agreement may result in the award of a follow-on production contract or transaction without the use of competitive procedures.”

2023 Other Transaction Guide

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Any agreement awarded off of this solicitation will include language requiring your company to confirm compliance with Section 889 of the John S. McCain National Defense Authorization Act for Fiscal Year 2019 (Pub. L. 115-232). If you are not able to comply with the law, the Government may not be able to award the agreement.

We Work With You

If we think there’s a good match between your solution and our DoD partners, we’ll invite you to provide us with a full proposal — this is the beginning of negotiating all the terms and conditions of a proposed prototype contract.

After a successful prototype, the relationship can continue and even grow, as your company and any interested DoD entity can easily enter into follow-on contracts.

Our Process

  1. We solicit commercial solutions that address current needs of our DoD partners.

  2. You send us a short brief about your solution.

  3. We’ll get back to you within 30 days if we’re interested in learning more through a pitch. If we're not interested, we'll strive to let you know ASAP.