N62645-17-R-0020_Amendment_0004_Combined_Synopsis_&_Solicitation.docx
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The purpose of this amendment is to replace FAR Clause 52.212-5 (JAN 2017) with FAR Clause 52.212-5 (DEVIATION 2013-O0019) (JAN 2017). Please note that this requirement is solicited under full and open competition as stated in the combined synopsis/solicitation introduction, the FBO posting, and the response to question #69 issued in Amendment 0002. No other changes are made.
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| File | Type | Posted |
|---|---|---|
| N62645-17-R-0020_Amendment_0003_Combined_Synopsis_&_Solicitation.docx | DOCX document | |
| N62645-17-R-0020_Amendment_0002_Combined_Synopsis_&_Solicitation.docx | DOCX document | |
| Attachment_3_Appendix_B.xlsx | XLSX spreadsheet | |
| Attachment_2_Appendix_A.xlsx | XLSX spreadsheet | |
| N62645-17-R-0020_Amendment_0001_Combined_Synopsis_&_Solicitation.docx | DOCX document | |
| N62645-17-R-0020_-_Combined_Synopsis_Solicitation.docx | DOCX document | |
| Attachment_1_Contract_Administration_Plan.docx | DOCX document |
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N6264517R0020
COMBINED SYNOPSIS/SOLICITATION
CAPABILITY-BASED MEDICAL TREATMENT FACILITIES
FOR
NAVY EXPEDITIONARY HEALTH SERVICES SUPPPORT
AMENDMENT 0004
The purpose of this amendment is to replace FAR Clause 52.212-5 (JAN 2017) with FAR Clause 52.212-5 (DEVIATION 2013-O0019) (JAN 2017). Please note that this requirement is solicited under full and open competition as stated in the combined synopsis/solicitation introduction, the FBO posting, and the response to question #69 issued in Amendment 0002. No other changes are made.
AMENDMENT 0003
The purpose of this amendment is to revise the delivery date for CLIN 0002. No other changes are made.
AMENDMENT 0002
The purpose of this amendment is to answer questions from potential offerors, revise the Statement of Objectives and to extend the closing date.
AMENDMENT 0001
The purpose of this amendment is to answer questions from potential offerors and to extend the closing date.
This is a combined synopsis/solicitation for commercial items prepared in accordance with FAR 12.6, Streamlined Procedures for Evaluation and Solicitation of Commercial Items. This announcement constitutes the only solicitation; proposals are being requested and a written solicitation will not be issued. It is the contractor’s responsibility to be familiar with the applicable FAR and DFARS clauses and provisions. The FAR and DFARS clauses may be accessed in full text at http://farsite.hill.af.mil/ current to FAC 2005-95.
The NAICS Code is 332312, with a business size standard of 500 employees.
This Request for Proposal (RFP) is a full and open competition for a Role 2 Enhanced (R2E) facility of Capabilities-Based Medical Treatment Facility that uses rigid-wall containers to provide a theatre medical facility which is clinically effective, as well as, being a rapidly deployable, independently operable, scalable, and modular expeditionary medical capability.
The solicitation number is N62645-17-R-0020.
This solicitation will result in one Firm Fixed Price contract.
Proposal Submission.
Proposals shall be submitted in accordance with the RFP (Addendum to 52.212-1 Instructions to Offerors – Commercial Items) to justin.d.robertson12.civ@mail.mil and heather.m.skimson.civ@mail.mil.
QUESTIONS AND ANSWERS
1. Offerors are required to provide a list of all essential durable medical equipment that is included to provide the operational functionality of the R2E as well as the total price for delivering that equipment. The 100% completed Solution will include this equipment but will undoubtedly be interpreted differently by each Offeror. Will the Government provide a list (with Part Numbers and Cage codes) of this durable medical equipment so that its evaluation of each Offeror’s proposal is consistent with the Streamlined Procedure under FAR 12.6?
Response: The Government will provide a list (Attachment 2 - Appendix A and Attachment 3 - Appendix B) of equipment currently in use in a similar soft shelter-based Role 2 Enhanced capability, however the list is not intended to be directive in nature but used as a guideline.
2. If the Government cannot provide this equipment list, how will offers that contain different and wide ranging equipment lists get streamlined by the Government for its evaluation?
Response: See response to question #1.
3. To more accurately estimate Life Cycle Costs how many patients and non-patients are expected to occupy the R2E facility on any given day? The formula for Total Water Cost, for example, contains daily water usage for patients and non-patients but does not specify the daily number of patients and non-patients who will use this water. A low estimate by an Offeror will result in a lower Life Cycle Cost.
Response: Up to 50 staff and 10 patients per day are expected to occupy the medical facility on any given day. Paragraph 2.2 of the Statement of Objectives (SOO) has been revised.
4. Section 2.2 states that the R2E will have the capability to hold at least 10 post-surgical patients. What is the maximum number of post-surgical patients that would need to be accommodated at one time?
Response: The maximum number of patients to be accommodated at one time is 10; 4 critical and 6 acute (see Statement of Objectives sections 2.2, 3.1.1, 3.1.12, and 4.1.23).
5. Section 4.1.16 states “The rigid-wall containerized capability shall have a singular standalone space to support morgue operations with storage capacity for up to 6 remains.” Is this standalone space to be included in the 9 TEU’s or can it be an additional, separate storage container?
Response: The morgue capability is not considered a medical space and, therefore, does not count against the 9 TEU objective or 12 TEU threshold. Paragraph 3.1.8 of the SOO has been revised.
6. Section 4.1.23 states the requirement for bathroom and shower service for a minimum of 10 patients. Do separate bathrooms and showers facilities need to be provided for male and female patients?
Response: No. Paragraph 4.1.23 of the SOO has been revised.
7. What is the maximum number of patients that would be using these bathroom/shower facilities?
Response: See response to question #4.
8. Can drawings be submitted on 11 x 17 pages in the proposal?
Response: Yes. ADDENDUM TO 52.212-1 INSTRUCTIONS TO OFFERORS: paragraph B. Proposal Format and Preparation Instructions, paragraph 5.a of the RFP has been revised.
9. Section 3.1.8. Please explain the rationale for establishing the objective of nine TEU’s. What was the basis for this objective?
Response: This objective is based upon observations and lessons learned.
10. Addendum C (Vol III)(2). LCC=I+Repl-Res+E+W+L(OM&R)+O; What is the assumed interest rate to be used to convert FV to PV?
Response: Please refer to the following website. https://www.whitehouse.gov/sites/whitehouse.gov/files/omb/memoranda/2017/m-17-10.pdf
11. Addendum C (Vol III)(2). LCC=I+Repl-Res+E+W+L(OM&R)+O; What is the depreciation method to be used?
Response: Depreciation shall be calculated using the straight-line method.
12. Addendum C (Vol III)(2). LCC=I+Repl-Res+E+W+L(OM&R)+O; What is the cost rate ($/gallon) of water consumption over time?
Response: The cost of generating a gallon of water for an MSC vessel is $2.38 per gallon. ADDENDUM TO 52.212-1, paragraph C(Vol III)(2) has been revised.
13. Addendum C (Vol III)(2). LCC=I+Repl-Res+E+W+L(OM&R)+O; What is the cost rate of electricity ($/W) consumption over time?
Response: The cost of generating electricity for an MSC vessel is $0.14 per kWh. ADDENDUM TO 52.212-1, paragraph C(Vol III)(2) has been revised.
14. Addendum C (Vol III)(2). LCC=I+Repl-Res+E+W+L(OM&R)+O; Is there an average amount of power usage per day to use in the calculations?
Response: Offerors shall estimate the average amount of power usage per day based on number of days/number of patients contained in solicitation and their knowledge of how their equipment functions or amount of power their equipment utilizes.
15. Addendum C (Vol III)(2). LCC=I+Repl-Res+E+W+L(OM&R)+O; Is the lifetime expectancy of the equipment representative of how long the equipment is expected to last or the useful life of the equipment?
Response: As stated in the solicitation in ADDENDUM TO 52.212-1 INSTRUCTIONS TO OFFERORS, paragraph C. Evaluation Criteria – Instructions, Volume III, paragraph 2, “The estimated lifetime expectancy for the containers is 20 years and the lifetime expectancy of the medical equipment is seven years.”
16. Section 3.1.4. Please clarify the equipment/capabilities provided by the external communications connection provided by the ship and host unit? We want to ensure compatibility for power, weight, space, etc.
Response: The connection type has been provided in section 3.1.5 of the SOO. The Government will not provide additional equipment beyond the connection.
17. Section 4.1.15. Please clarify capacity needed for food and perishable refrigeration, since the previous RFP requirements for Mess facilities are no longer requirements for the system.
Response: There is no requirement in this RFP to provide food service capability, so no need for food refrigeration.
18. Is there an estimated start date to use for CLIN0001? We need a start date to determine our costs.
Response: The estimated award date for the contract is 1 October 2017 and the delivery date for CLIN 0001 is 29 December 2017.
19. Will the government award CLIN0001 and CLIN0002 at the same time?
Response: The contract will be awarded with both CLINs. The CLINs have separate delivery dates and payments will not be made until delivery is made.
20. If CLINs not awarded at the same time, will long lead items be authorized prior to award of CLIN0002?
Response: See response to question #19.
21. Addendum C (Vol III)(1)(c). Volume I Tab 3 milestones are requested. However, in same section Volume III requirements it states “Note: Milestone payments will not be provided” Please clarify.
Response: Yes, milestones are required as a part on an offeror’s Time Phased Project Plan. Additionally, Volume III requires offers to propose estimated prices that crosswalk to the completion of specific tasks identified in the Time Phased Project Plan submitted with Volume II. This is to help the government understand how offerors calculated their total price. Milestone payments will not be made. Only two payments will be made; one each upon delivery of CLIN 0001 and CLIN 0002.
22. Section 3.1.1. The requirement is for six casualties to arrive at once. Can the ICU/acute care beds be utilized for patient/casualty receiving or is it assumed that the patient receiving area needs its own beds?
Response: The casualty receiving area is separate from the intensive care unit and acute care ward.
23. Addendum C (Vol III)(1)(c). Solicitation N62645-16-R-0039 Offeror’s were requested to propose milestone payments. It appears the government changed the requirement? Please clarify.
Response: Each solicitation stands alone. Under this solicitation and resultant contract milestone payments will not be authorized.
24. Payment type. The Solicitation is Firm Fixed Price with WAWF. However, the acceptance criteria associated with the deliverables do not appear to be clearly defined. In order to alleviate uncertainty, would the government accept a proposed milestone payment schedule?
Response: Milestone payments will not be made under the resultant contract.
25. Addendum C (Vol III)(1)(c). Paragraph C under Volume III requirements it states “Note: Milestone payments will not be provided”. Will the government entertain a potential milestone payment schedule prior to contract award?
Response: Milestone payments will not be made under the resultant contract.
26. Section 3.1.1. Previous RFP provided a list of equipage. No list was provided with the new request for proposal. Will the customer provide the same equipage list from the previous request for proposal?
Response: See response to question #1.
27. Addendum C (Vol III)(1)(c). Paragraph C under Volume III requirements it states “Note: Milestone payments will not be provided”. If Milestone payments are not acceptable, then would the government entertain other forms of payment during contract performance prior to final acceptance of deliverables?
Response: Contract financing payments will not be made under the resultant contract.
28. Are soft-sided access or connecting walkways acceptable?
Response: Access and/or connecting walkways must meet all applicable American Bureau of Shipping and U.S. Coast Guard requirements per RFP paragraph 4.1.4.
29. What is the Temperature Range Operation required? It appears that two different ranges are listed between Section 4.1.8 and 4.1.12.
Response: The capability must be able to operate in temperatures ranging from -25 degrees Fahrenheit to +140 degrees Fahrenheit. Section 4.1.12 of the SOO has been revised.
30. Section 4.1.15 notes “separate monitored refrigeration for food and other perishables”. What are the associated food and perishable requirements, if any?
Response: See response to question #17.
31. Is the morgue space considered part of the medical capability?
Response: See response to question #5.
32. Per 3.1.6, will the network need to be able to perform dynamic routing through protocols such as OSPF or EIGRP?
Response: ISNS and CANES are the two most common networks used by Navy. Most modern networks use some sort of dynamic routing protocol, usually either OSPF and/or EIGRP depending on whether or not there are CISCO products in the mix.
33. Per 3.1.5, will the networks only have 1 point of egress through the router that will be connected, and if so, what types of egress circuits will be used?
Response: There could be multiple egress points and the circuit types will depend upon the environment and the Service providing base operating support.
34. Per 3.1.4, what are the hardware requirements for the computers and networking equipment to connect to the TMIP-M and JOMIS systems?
Response: Section 3.1.4 of the SOO has been revised.
35. Per 3.1.6, which modules must have the necessary equipment to connect to the SIPRnet? Which modules must have the necessary equipment to connect to the NIPRnet?
Response: The command and control, administration, medical logistics, and biomed repair container(s)/area(s) require two (2) SIPRnet connections and two (2) NIPRnet connections each. All other containers require at least 2 NIPRnet connections per sections 4.1.19 and 4.1.25 of the SOO.
36. Per 4.1.19, what kinds of radios are required?
Response: Secure portable radios are required. Section 4.1.19 of the SOO has been revised.
37. What is the required bandwidth for the containers uplinks to the nets via external communication connections?
Response: The bandwidth capability shall support 10GB. See section 3.1.4 of the SOO.
38. What rooms will require SIPR connections?
Response: See response to question #35.
39. Although the TEU’s can be repurposed for different functions, is there a defined preference for how they should best be arranged to transfer patients between staging elements?
Response: No, the Government expects and desires industry innovation to achieve a solution to meet the specified performance objectives.
40. What medical equipment does the Government or its SME’s recommend for its interpretation of a 100% Solution?
Response: In addition to the response to question #1, the Government expects and desires industry innovation to achieve a solution, including equipment not necessarily already employed in similar capabilities, to meet the specified performance objectives.
41. Can the successful Offeror’s proposed medical or communications equipment be modified after an award?
Response: Upon mutual agreement of the parties an equal to or greater than substitution/replacement may be considered if determined to be within scope of the contract.
42. Since there are a significant number of questions pending response and these responses may greatly affect the design of the system, can the government please provide at least a 2 week extension on the due date to allow for time to incorporate the answers provided into the proposal?
Response: The closing date of the solicitation has been extended. Please see ADDENDUM TO 52.212-1 INSTRUCTIONS TO OFFERORS: paragraph A.6.
43. Since the answers to questions may result in additional questions, can the deadline to submit questions be extended?
Response: The closing date of the solicitation has been extended. Please see ADDENDUM TO 52.212-1 INSTRUCTIONS TO OFFERORS: paragraph A.6.
44. 3.1.2 The rigid-wall containerized medical capability shall contain the necessary medical equipment and supplies to be able to stabilize post-surgical cases for evacuation to definitive medical care.
Does the government intend on providing a bill of materials of what medical equipment and supplies it desires as a minimum requirement?
Response: See responses to questions #1 and #51.
45. 3.1.8 - The medical capability shall be packed, loaded and transportable in the fewest number, with an objective of no more than nine, 20 foot equivalent units (TEU’s), not including TEU’s necessary for storage of 15 days of supply.
45.a. Does the government plan on including the spaces for administration, medical logistics, biomedical repair, and Command and Control sections in the nine, 20 foot equivalent units (TEU’s) medical capability?
Response: Yes.
45.b. If the nine TEU is the objective does the government have a threshold?
Response: The TEU threshold is 12, not including those required for storage and morgue. Section 3.1.8 of the SOO has been revised.
46. 4.1.22 - The rigid-wall containerized capability shall have universal component interlocking capability to connect or disconnect allowing for multiple complexing configurations within the design, consistent with envisioned operations within the hold of a cargo ship. Patients and staff shall be able to transition from one location to another without exiting the rigid-wall container capability.
Is the government acceptable to soft sided boots that seal the connections between containers?
Response: See response to question #28.
47. 3.1.17 - The rigid-wall containerized system shall be equipped with 208V, 30 amp 3 phase capability and water recovery technology to support sterilization procedures.
Does the government mean that the water recovery only pertains to the sterilization system that is used to sterilize the medical instruments and not water recovery for any other requirement like grey waste water?
Response: Yes, water recovery only pertains to sterilization.
48. 3.1.11/4.1.10 - The rigid-wall containerized capability tie downs, secure tracks or other technology to secure equipment, furniture, etc. design shall have the flexibility to support various configurations to support scalability and complexing (i.e., snapping together) of multiple MSFPs. For example, a container initially outfitted with equipment to support a specific function (e.g., radiology, laboratory, etc.) may be repurposed to support a different function simply by relocating the equipment from one container to another.
48.a. Is the specified requirement that the design shall have the flexibility to support multiple configurations tied to complexing capabilities of specific MTF functional modules or the ability to shift the functional use of individual modules, i.e., OR can be shift to support ICU or ACU or vice versa or both?
Response: The rigid-wall containerized capability should accommodate shifting of functional areas between containers (i.e., what was configured as OR can be reconfigured as ICU) and multiple complexing configurations (i.e., each container has multiple access/connection points).
48.b. Please specify which containers are medical capability that need to be interchangeable and which containers are considered non-medical that will need to be interchangeable? ie: medical capability containers are the OR, ICU, ACU & Casualty Receiving Point. Non-medical are Admin, C2, Lab etc?
Response: The Government did not specify containers need to be interchangeable, but did specify flexibility within and between containers to facilitate various configurations, scalability and complexing. Containers for storage, morgue, and non-patient care areas (administration, command and control, biomed repair, medical logistics) need not be configurable as patient care areas. The only containers that are not considered part of the medical complex are those used for storage and morgue.
49. 4.1.17 - The rigid-wall containerized capability shall meet all ABS standards for fire alarm notification system that can be integrated with existing ship alarm systems and vice versa; each container shall meet all ABS standards for operable mounted 10B NFPA fire extinguishers and carbon monoxide detectors.
What is the existing shipboard alarm notification system with specific connection types to support MTF solution alarm system integration?
Response: Configuration of the shipboard alarm notification system differs from ship to ship. For the ship classes in consideration for this mission the alarm notification system will fall in to one of the following categories: addressable serial communication (RS-232 or RS-485), MODBUS TCIP/IP or Programmable Logic Control (PLC). Coordination with ship’s current fire control system shall be required after contract award. Section 4.1.17 of the SOO has been revised.
50. 4.1.19 - The rigid-wall containerized capability shall have organic internal communication (phones, radios, intercom) that must integrate with host unit/ship general and emergency communications systems and shall be designed with multiple ports for server and network connections; a minimum of 2 stations per container.
What is the existing shipboard general and emergency communications systems with specific connection types to support MTF solution voice/data communications system integration?
Response: Current connection types of the shipboard general and emergency communications are either RJ45 or RJ11. The shipboard system has been updated from analog to digital by way of VOIP (voice over internet protocol). Section 4.1.19 of the SOO has been revised.
51. 4.1.11 The rigid-wall containerized capability shall have the capacity to store all medical equipment, as well as 15 days of supply of medical, surgical, and pharmaceutical consumables to include a combination safe to secure controlled narcotics and administrative supplies. The safe should be at least large enough to hold controlled narcotics sufficient for the operation of the R2E capability for 15 days.
Does the government intend to issue a list of what they require for a 15 day of supply of medical, surgical, and pharmaceutical consumables to include controlled narcotics and administrative supplies?
Response: The Government will provide a list of consumables currently in use in a similar Role 2 Enhanced tent-based capability, however the list is not intended to be directive in nature but used as a guideline.
52. 4.1.23 The rigid-wall containerized capability shall provide central laundry service (capable of washing soiled medical linen, scrubs, gowns and the like (Center for Disease Control min 160 degrees Fahrenheit-25 mins), bathroom and shower service for a minimum of 10 patients. Approximately 100 pounds per day.
What are the design parameters - number or personnel/patients per latrine, shower, and laundry that would meet the government’s needs? Do the showers and latrines need to be handicap accessible / accommodate a wheel chair? Are two latrines, two showers, two sinks and 1 each washer/dryer a sufficient quantity for this requirement?
Response: The latrines and showers are for patients only. As specified elsewhere, the facility must support up to 10 admitted patients per day. Yes, showers and latrines must be handicap accessible, but do not have to accommodate wheelchairs. The quantities of showers, latrines, washers and dryers should be sufficient to meet the stated performance objectives. Section 4.1.23 of the SOO has been revised.
53. 3.1.5 The rigid-wall containerized capability shall maintain voice communications with supported units’ evacuation and command nets via external communications connections provided by the host unit/ship.
Is there a standard connection type that is provided by the host unit/ship?
Response: The connection type for voice communication is a RJ45 cable.
54. 3.1.6 The rigid-wall containerized capability shall provide connectivity to shore via Secret Internet Protocol Router Network (SIPRnet) and Non-classified Internet Protocol Router Network (NIPRnet) sufficient for patient movement and patient regulation activities. The rigid-wall containerized capability must connect to the Theater Medical information Program Maritime (TMIP-M) network and TRANSCOM Regulating and Command & Control Evacuation System (TRAC2ES).
Will the host unit/ship provide the operational SIPR/NIPR communication network for connectivity or is a standalone satellite communication system required to provide this capability?
Response: The host unit/ship will provide network connectivity.
55. 3.1.12 The rigid-wall containerized medical capability shall provide no less than (93% +/-3%) portable oxygen. The rigid-wall containerized capability shall have portable medical oxygen generation capability sufficient to support 7 surgeries per day, 10 post-surgical patients (up to 4 ICU patients), and filling oxygen bottles for evacuation of up to 2 patients per day.
Is the desired minimum number of liters of oxygen required to support 7 surgeries per day, 10 post-surgical patients (up to 4 ICU patients), and filling oxygen bottles for evacuation of up to 2 patients per day? Is there a requirement for additional gases?
Response: The Government expects and desires industry innovation to achieve a solution to meet the specified performance objectives.
56. 3.1.13 The rigid-wall containerized communication capability shall provide network display capability (monitors) to review medical information throughout the R2E medical facility.
Is there a minimum or desired size of the display to provide sufficient/best ability to review medical information? Is this a workstation that requires a keyboard, mouse and computer as well?
Response: See response to question #34.
57. 4.1.11 The rigid-wall containerized capability shall have the capacity to store all medical equipment, as well as 15 days of supply of medical, surgical, and pharmaceutical consumables to include a combination safe to secure controlled narcotics and administrative supplies. The safe should be at least large enough to hold controlled narcotics sufficient for the operation of the R2E capability for 15 days.
Is there a recommended loadout list for the 15 days of supply of medical, surgical, and pharmaceutical consumables, to include the controlled narcotics, required for continued operations that would allow a better determination of containerized and secure safe storage configuration and capacity?
Response: See response to question #51.
58. 4.1.20 The rigid-wall containerized capability shall be capable of receiving and distributing power from the host ship or unit to the entire complex to include electrical cabling, plugs, adapters, power panels, central digital monitoring and the necessary redundant equipment for independent operations or scaled to increase capacity.
Is the contractor required to provide the connecting cable(s) for receiving power from the host ship or unit? If yes, what type of connectors are used to plug into host ship/unit power?
Response: Yes, cables must be provided by the contractor with connections in accordance with MIL-C-22992 TYPE CONNECTORS.
59. 4.1.24 The rigid-wall containerized capability shall have the means to receive and distribute potable water from host ship/unit as well as to transfer hazardous/medical waste (estimated at 45 ppd) and grey/black water to the host ship or unit for collection and/or disposal.
Is the contractor required to provide the connecting hoses to transfer grey/black water to the host ship or unit? If yes, what type of hose connectors are used to integrate into host ship/unit system?
Response: Yes, hoses must be provided by the contractor. Potable water hoses will have 1.5” hoses with cam and groove (CAMLOCK) fittings and 2” waste water (black water) hoses with 2” CAMLOCK fittings. There should be male-to-male and female-to-female adapters provided for both as well. Section 4.1.24 of the SOO has been revised.
60. 4.1.16 The rigid-wall containerized capability shall have a singular standalone space to support morgue operations with storage capacity for up to 6 remains. Container should be able to refrigerate at standard morgue temperatures of 34 to 40 degrees Fahrenheit or 1.1 to 4.4 degrees Celsius.
Please confirm that the government does not require the standalone morgue unit to be physically connected to the medical complex?
Response: The morgue does not need to be physically connected to the medical complex.
61. 4.1.25 The rigid-wall containerized capability shall include spaces for administration, medical logistics, biomedical repair, and Command and Control sections. A minimum of a 3 network drops, monitors, furniture and workstations for each section are required.
Please confirm that 3 network drops, monitors, furniture and workstations are required for each of the 4 sections: administration, medical logistics, biomedical repair and C2, for a total of 12 sets?
Response: See response to question #35.
62. 4.1.15 The rigid-wall containerized capability shall provide monitored refrigeration capability to store up to 60 Packed Red Blood Cells or liquid plasma units, pharmaceuticals and other medical supplies at 1 to 6°C, and separate monitored refrigeration for food and other perishables.
4.1.15 calls out a separate monitored refrigerator for food. What size refrigerator for food and other perishables will be required?
Response: See response to question #17.
63. 4.1.12 The rigid-wall containerized capability shall be capable of being cooled or heated independently or as part of the integrated grouping capable of operating in temperatures ranging from 25°F to 140 °F.
Please confirm that each container is required to have its own self-contained heating and cooling system as part of the container system and can also be connected to central heating/cooling systems typically found in FOBs?
Response: Yes, each container is required to have its own self-contained heating and cooling system as part of the container system and can also be connected to central heating/cooling systems provided by host unit/ship.
64. We request a 30-day extension to the current deadline to allow our team to prepare a comprehensive solution for the proposed solicitation.
Response: The closing date of the solicitation has been extended. Please see ADDENDUM TO 52.212-1 INSTRUCTIONS TO OFFERORS: paragraph A.6.
65. Regarding the estimated Life Cycle Costs (LCC) in the Price Volume, is there a specific format in which you want this information presented? Do you want a breakdown of estimate costs for each of the required values in the LCC formula?
Response: No breakdown of the information is required. Offerors shall provide the completed formula and LCC total.
66. Regarding the Time Phased Project Plan, how detailed of a plan do you want offerors to provide? Can you please provide greater detail on the information you seek in terms of “schedule, interdependencies, and milestones?”
Response: It is each offeror’s discretion as to how they choose to propose all the Technical requirements within the 50 page limitation. The purpose of the Time Phased Project Plan is for the offeror to demonstrate understanding of the requirement and to convey the offeror’s plan to achieve the solution. In addition, the offeror shall propose estimated prices that crosswalk to the completion of specific tasks identified in the Time Phased Project Plan submitted with Volume II in accordance with ADDENDUM TO 52.212-1 INSTRUCTIONS TO OFFERORS: C. Evaluation Criteria – Instructions, Volume III –Business/Price paragraph c.
67. Can you please provide a full list of the required rooms/facilities (e.g. Operating Room, 6 Bed Acute Care, ICU, x-ray, etc.) that make up the objective nine TEU “medical capability”?
Response: No, the Government expects and desires industry innovation to achieve a solution to meet the specified performance objectives.
68. Please confirm which MIL-M-81957(AS) standard is required as per section 4.1.8. A search of the Assist website revealed the list of standards below, but none contain the standard with the "AS" ending as referenced in 4.1.8. Please advise.
Response: The mil spec listed is antiquated. Section 4.1.8 of the SOO has been revised.
69. Small businesses will be disadvantaged since contract financing payments, progress payment and milestone payments will not be made under the resultant contract. Small businesses will be unduly burdened by having to absorb the lengthy and significant cash crunch that will precede the government’s payment. Their borrowing capacity to grow will be impaired and opportunities to fund other projects will be diminished. Please explain how the government intends to make this solicitation fair to all offers.
Response: This solicitation is for a firm fixed price contract which is not a contracting vehicle that supports financing options. The Government’s need is for an end state capability that is not conducive to separate deliverables. This requirement is for full and open competition and not set aside for small business, however, small businesses are encouraged to submit a proposal.
70. Section 3.1.17 and the answer to question number 47 states that the water recovery shall only pertain to sterilization. What should the capacity and output of this system be?
Response: The Government expects and desires industry innovation to achieve a solution to meet the specified performance objectives.
Exhibit/Attachment Table of Contents
| DOCUMENT TYPE |
| DESCRIPTION |
| PAGES |
| DATE |
| Attachment 1 |
| Contract Administration Plan |
| 15 |
| Attachment 2 |
| Appendix A |
22-MAY-2017
| Attachment 3 |
| Appendix B |
22-MAY-2017
| ITEM NO |
| SUPPLIES/SERVICES |
| QUANTITY |
| UNIT |
| UNIT PRICE |
| AMOUNT |
| 1 |
| Each |
R2E 100% Project Solution
FFP
Role 2 Enhanced (R2E) Medical Facility 100% Project Solution includes the Narrative Response, 100% completed Design Drawing, Time Phased Project Plan, and a Cybersecurity Discussion.
FOB: Destination
NET AMT
| ITEM NO |
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R2E Medical Facility
FFP
Marinized rigid-wall container based Role 2 Enhanced (R2E) Medical Facility capable of being assembled and employed to provide primary surgery, resuscitative trauma surgery, emergency medicine, and associated ancillary capabilities.
NET AMT
STATEMENT OF OBJECTIVES
1.1 Overall Objective: This Request for Proposal) is to engage industry to design an innovative outfitting assembly and configuration solution for a complete marinized rigid-wall container based Role 2 Enhanced (R2E) medical facility capable of being assembled and employed to provide primary surgery, resuscitative trauma surgery, emergency medicine, and associated ancillary capabilities. The overarching objective of the rigid-wall Containerized Medical Capability is to provide a medical capability that delivers a fully functional, immediately employable upon emplacement, responsive, deployable, modular and scalable expeditionary medical capability that is clinically effective, incorporating material alternatives into rigid-wall containers afloat and ashore.
1.2 Expectation: The contractor will prepare a written proposal for review by the Government based on the performance objectives and constraints as stated in sections 3 and 4 of the Statement of Objectives.
2.1 Background: The US Navy intends to accomplish an evolutionary modernization of the current Expeditionary Medical Facility-150 bed (EMF-150) capability into a modular and scalable capability called “Capabilities-Based Medical Treatment Facility” (CB-MTF). CB-MTF is a family of capabilities that delivers rapidly deployable, task organized and scalable expeditionary health service support in the afloat or ashore environments in order to support designated combatant command (CCMD) missions across the full range of military operations. The CB-MTF is clinically effective and comprised of a small number of Medical Standard Force Packages (MSFP) that are manned, trained, equipped and certified ready for operations. Inherent in the full CB-MTF capability (known as CB-MTF Major Combat Operations (MCO)), is a Role 2 Enhanced (R2E) capability, the subject of this RFP, that can operate, either afloat in the hold of an available cargo ship or ashore with a host unit. CB-MTF R2E is a Role 2 Enhanced medical facility as defined in Joint Publication 4-02, Health Service Support (http://www.dtic.mil/doctrine/new_pubs/jp4_02.pdf ).
2.2 Vision: Under the CB-MTF Concept of Operations (CONOPS), the R2E is envisioned as a modular capability established in rigid-walled containers that can be configured as necessary to operate afloat in the cargo hold of select Military Sealift Command (MSC) ships or ashore. The R2E capability operating afloat or ashore shall be dependent on the host platform or unit for utilities (power, water, waste handling/disposal, etc.) and hoteling services (berthing, messing, laundry, hygiene, etc.) for approximately 50 staff. The R2E will have 2 operating room tables to support up to 7 surgeries per day, and have the capability to hold up to 10 post-surgical patients including 4 critical or Intensive Care Unit (ICU) and 6 Acute Care patients, until they can be moved to a higher level of care. The R2E will stand up and operate with medical supplies for up to 15 days without resupply.
2.3 The Role 2 Enhanced (R2E) facility is a CB-MTF Core Attribute: The CB-MTF MCO design is comprised of four separate modular MSFP components. These four components are Role 2 Light Maneuver, R2E, Role 3, and a 100 ward bed augment package. Each MSFP is capable of being transported and operated independently of the others. The CB-MTF provides a scalable capability that will enable the MSFP components to transition from light to heavy casualty throughput by connecting, complexing or snapping one or more MSFP components together to incrementally increase capability and capacity culminating in all components combining to provide the CB-MTF MCO capability. They are configurable to suit major operations or campaigns, crisis response and limited contingency operations, military engagement, and security cooperation missions. The CB-MTF is centered on clinical effectiveness to assure positive outcomes and survivability of the patient. It shall conform to clinical practice guidelines for surgical and other health service support, which includes stabilization, triage, treatment, evacuation and conformance to clinical practice. The CB-MTF deployable capability relies on a standardized universal component rigid-wall container design; allowing for flexibility, ease of transport, compatibility with rapid intermodal handling platform (air, sea, truck and rail) and adaptability of operating afloat or ashore.
3.1 Performance Objectives: The performance objectives described herein are the basis for offerors to understand the overall scope of this requirement from the Government’s perspective. It is expected that the offeror will take the Performance Objectives and propose their best technical approach to meeting the objectives described herein. Core Role 2E Functions include:
| • | Primary Surgery: Allied Joint Pub 4.10(A) defines Primary Surgery as: “the surgery directed at repair of the local damage caused by wounding, rather than correcting the generalized effects” as opposed to Damage Control Surgery which applies the concept that “only the minimum is done to deal with life- threatening problems” when the casualty’s physiological limits can’t tolerate primary surgery. |
| • | Casualty receiving, triage, emergency medical support, and resuscitative trauma surgery |
| • | Complex medical and surgical care |
| • | Critical care (respiratory therapy, and post-anesthesia care to a variety of trauma, surgical, and medical patients) |
| • | Advanced trauma life support (ATLS) |
| • | Laboratory and other ancillary services, medical C2 (command and control), administration, medical logistics support, |
| • | Oxygen generation and blood operations |
3.1.1 The rigid-wall containerized medical capability design shall include a fully functional, clinically effective Operating Room (OR) with two tables, accomplishing up to 7 surgeries per day. It shall have 4 ICU beds and a 6 bed acute care ward capability with sufficient supplies to be sustainable for 15 days before resupply. It shall also have a patient/casualty receiving capability sufficient to assess a minimum of six (6) patients/casualties simultaneously.
3.1.2 The rigid-wall containerized medical capability shall contain the necessary medical equipment and supplies to be able to stabilize post-surgical cases for evacuation to definitive medical care.
3.1.3 The rigid-wall containerized capability shall allow for unencumbered reception of patients, casualties, and free-flow movement for staff and patient transport via standard military patient carrying items such as field litter, gurney, wheelchair or stretcher throughout the structure. The minimum passageway and doorway must be able to accommodate a 33.5 inch wide gurney that is wheeled with the side rails up.
3.1.4 The rigid-wall containerized capability shall have the information technology hardware and communications to support current, Theater Medical Information Program Maritime (TMIP-M), and future, Joint Operational Information System (JOMIS) theater medical information systems. These systems create, edit, store and transmit data regarding patient location, patient status, telemedicine diagnosis and therapy, medical regulation and medical logistics via external communication connections provided by the host ship/unit. See table below for minimum hardware requirements.
| Platform |
| Client Only |
(New in I2 R3 SP1) Standalone / Medium Server (Up to 15 clients) Large Server (More than 15 clients)
Processor (64-bit system)
| 2.53 GHz Core 2 Duo or higher |
| 1-4 Socket CPU with 2.66 GHz Dual Core Processors, 2.40 GHz Quad Core Processors or higher |
| 2-4 Socket CPU with 2.80 GHz Dual Core Processors, 2.53 GHz Quad Core Processors, or higher |
| Memory |
| 4 GB |
| 10 GB |
| 16 GB |
Hard Disk
(5400 RPM)
80 GB
| 400 GB |
| 900 GB |
(SCSI – RAID 5)
| Backup Devices |
| Any Microsoft Windows-compatible high capacity and high speed device capable of using tapes that are at least 40 GB uncompressed. |
| Pointing Device |
| Any Microsoft Windows-compatible device |
| DVD/CD |
| Any Microsoft Windows-compatible device. For backup to external drive, write capability of at least 8X-DVD/40X-CD required. |
| CAC |
| Any DoD approved Smart Card Reader |
| Scanners |
| Microsoft Windows-compatible scanner |
AHLTA-Theater – A DoD approved barcode scanner with the capability of scanning Code 39 and PDF417.
Tested product – Metrologic Focus MS1690
| Display |
| SVGA (1024 x 768 or higher) |
| Ports |
| 4 USB 2.0, SD Card Reader |
| Network Interface |
| 1 Gbps |
| 1 Gbps with fail-over and load balancing |
3.1.5 The rigid-wall containerized capability shall be capable of maintaining voice communications with supported units’ evacuation and command nets via external communications connections provided by the host unit/ship. The connection type for host ship voice communication is a RJ45 cable.
3.1.6 The rigid-wall containerized capability shall provide connectivity to shore via Secret Internet Protocol Router Network (SIPRnet) and Non-classified Internet Protocol Router Network (NIPRnet) sufficient for patient movement and patient regulation activities. The rigid-wall containerized capability must connect to the Theater Medical information Program Maritime (TMIP-M) network and TRANSCOM Regulating and Command & Control Evacuation System (TRAC2ES).
3.1.7 The rigid-wall containerized capability shall provide uninterruptible power supply (UPS) backup sufficient for powering emergency lighting in all containers independent of each other for at least 12 hours in the event host ship/unit power is interrupted. The UPS shall be able to operate in the same conditions as specified in 4.1.6.
3.1.8 The medical capability shall be packed, loaded and transportable in the fewest number, with an objective of nine and a threshold of 12, 20 foot equivalent units (TEU’s), not including TEU’s necessary for storage of 15 days of supply and morgue (see paragraph 4.1.16 below). TEUs associated with administration, command and control, biomed repair, and medical logistics are considered part of the medical capability and do count against the TEU objective/threshold. Transport platforms include aircraft (C-130, C-17 or C-5), train, ground or ship.
3.1.9 Packing and methods of preservation shall be marinized to protect material against environmentally induced corrosion and deterioration, physical and mechanical damage and other forms of degradation during storage and multiple handling as well as when employed.
3.1.10 The entire rigid-wall containerized medical capability shall be capable of being rapidly erected and set up to begin medical operations within 30 consecutive hours by the fewest number of individuals feasible in both the afloat and ashore environments. Ground leveling capability for the containers is required for when employed ashore.
3.1.11 The rigid-wall containerized capability modules shall have a scalability component that will allow it to be complexed together with other configurations increasing its capacity and capability. Ships being considered to host this capability include the Bob Hope, Watson, and Gordon Classes of MSC cargo ships. There is variation between and within these classes of ships and, therefore, the flexibility of multiple configurations is required. The R2E capability shall allow for the greatest possible flexibility in reconfiguration or complexing variations in order to improve the ability to meet various ship board designs. Each rigid-wall container of the R2E capability must be capable of securing to the deck of the ship for sea worthiness.
3.1.12 The rigid-wall containerized medical capability shall provide no less than (93% +/-3%) portable oxygen. The rigid-wall containerized capability shall have portable medical oxygen generation capability sufficient to support 7 surgeries per day, 10 post-surgical patients (up to 4 ICU patients), and filling oxygen bottles for evacuation of up to 2 patients per day.
3.1.13 The rigid-wall containerized communication capability shall provide networked workstations with no less than 19” display capability (monitors) to review medical information throughout the R2E medical facility.
3.1.14 The rigid-wall containerized capability shall have an internal intercom system, external public announcement capability, and internal phone system.
3.1.15 The rigid-wall containerized medical capability shall provide Basic Laboratory procedures in hematology, urinalysis, microbiology, and serology, limited Blood Banking capability (storage for up to 60 units in some combination of packed red blood cells and fresh frozen plasma); no frozen red blood cells capability will be required.
3.1.16 The rigid-wall containerized capability shall provide other ancillary services to include a pharmacy equipped to securely store and dispense medications including controlled substances, radiology equipment consisting of a mobile radiographic x-ray unit, and a portable ultrasound system.
3.1.17 The rigid-wall containerized capability shall be equipped with 208V, 30 amp 3 phase capability and water recovery technology to support sterilization procedures.
4.1 Constraints: The Role 2E rigid-wall containerized medical capability employed afloat/ashore shall conform to following criteria without Government Furnished Equipment (GFE); all included equipment should be new.
4.1.1 The rigid-wall containerized capability shall provide basic secondary health care, built around primary surgery, an intensive care unit, and acute care ward beds.
4.1.2 The rigid-wall containerized capability may be comprised of any combination of non-expandable or expandable quad-, tri-, bi-, and 20’ International Standard Organization (ISO) containers, but must meet the ISO (1496/1) standards. No container (including expandable containers when closed) may exceed 20 feet in length, 8 feet in width, and 8 feet in height to allow intermodal freight transport (rail, ship, truck and air).
4.1.3 The rigid-wall containerized capability shall meet International Convention for Safe Containers (CSC) certification. For storage and transport it will be certified stackable 9 high. If a CSC certified container is structurally modified in any way, it must be recertified prior to government acceptance.
4.1.4 The rigid-wall containerized capability shall meet all applicable American Bureau of Shipping (ABS) and United States Coast Guard (USCG) requirements.
4.1.5 The rigid-wall containerized capability shall have a minimum of two each removable tie-down rings with required cables, straps and connectors (per expandable wall) and four each cables, straps and connectors (one per ISO post) to allow for securing it to the deck of a ship and/or securing to the ground with ground anchors during operation underway or in high winds. These rings and cables shall not interfere with the capability for multiple complexing configurations or entry, exit ramps into and out of containers within the design.
4.1.6 When not in storage/transport configuration, but configured for employment as a Role 2E MTF, rigid-walled containers providing patient care areas may not be stacked. However, rigid-walled containers providing non-patient care areas (e.g., medical supply, administration, etc.) may be stacked up to three high, with approved scaffolding.
4.1.7 The rigid-wall containerized capability (packed out ready for storage/transport) shall not exceed maximum weight of 20K pounds per TEU in its closed position ready for transportation. Below is a list of the container operational requirements:
4.1.8 Below is a list of the container operational requirements:
| 1. | ISO/ANSI Specs ISO 1496/1 and ANSI MH5.1, 5.1.1 and 5.4 ASTM Designation: PS 27 – 95 | |
| 2. | Exterior Dimensions; 96in. high, 96in. wide, 238 1/2 in. long | |
| 3. | Roof Loads; Live load of 660 lbs on an area 24 in. by 12 in.; or 75 lb./ft. 2 uniform snow load | (minimum) |
| 4. | Floor Loads; 138 lbs/ft2 uniform (minimum) | |
| 5. | Heat Transfer; Insulated to provide a heat transfer coefficient of 0.25 BTU/hr. ft. 2/°F (maximum | rate of loss) |
| 6. | Temperature Range Operation: -25°F to + 140°F | |
| 7. | Temperature Range Storage: -65°F to + 160°F | |
| 8. | Container/Shelter shall have built-in fork lift provisions |
4.1.9 The rigid-wall containerized capability, when expanded, shall have the capability of securing all equipment, furniture, etc. by way of tie-downs, secure tracks or other technology that allows for continued operations afloat while underway at sea.
4.1.10 The rigid-wall containerized capability tie downs, secure tracks or other technology to secure equipment, furniture, etc.
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