Solicitation W81K00-20-Q-0084 Amendment 0001.pdf

W40M USA HLTH CONTRACTING ACT

REGIONAL HEALTH CONTRACT OFF CENTRAL

POC: BRENDA FERJAK

1650 COCHRANE CIRCLE, BLDG7500

FORT CARSON CO 80913-4604

0011417826

AMENDMENT OF SOLICITATION/MODIFICATION OF CONTRACT

Except as provided herein, all terms and conditions of the document referenced in Item 9A or 10A, as heretofore changed, remains unchanged and in full force and effect.

15A. NAME AND TITLE OF SIGNER (Type or print)

30-105-04EXCEPTION TO SF 30

APPROVED BY OIRM 11-84

STANDARD FORM 30 (Rev. 10-83) Prescribed by GSA

FAR (48 CFR) 53.243

The purpose of this amendment is to:

1. Update Line Item Description for CLINS 0001AA, 1001AA, 2001AA, 3001AA and 4001AA.

2. Update some of the technical specs listed in the Statement of Work. Paragraphs 5.2, 5.2.4, 5.2.5, 5.2.27, 5.2.29, 5.2.38 and 5.2.39 preceeded by three asterisks (***) contain revisions. All other paragraphs remain unchanged.

The solicitation receipt of offers is not extended w ith this amendment.

1. CONTRACT ID CODE PAGE OF PAGES

1 44

16A. NAME AND TITLE OF CONTRACTING OFFICER (Type or print)

16C. DATE SIGNED

BY

16B. UNITED STATES OF AMERICA15C. DATE SIGNED15B. CONTRACTOR/OFFEROR

(Signature of Contracting Officer)(Signature of person authorized to sign)

8. NAME AND ADDRESS OF CONTRACTOR (No., Street , County, State and Zip Code) X W81K0020Q0084

X 9B. DATED (SEE ITEM 11)

21-May-2020

10B. DATED (SEE ITEM 13)

9A. AMENDMENT OF SOLICITATION NO.

11. THIS ITEM ONLY APPLIES TO AMENDMENTS OF SOLICITATIONS

X The above numbered solicitation is amended as set forth in Item 14. The hour and date specified for receipt of Offer is extended, X is not extended.

Offer must acknowledge receipt of this amendment prior to the hour and date specified in the solicitation or as amended by one of the following methods:

(a) By completing Items 8 and 15, and returning 1 copies of the amendment; (b) By acknowledging receipt of this amendment on each copy of the offer submitted;

or (c) By separate letter or telegram which includes a reference to the solicitation and amendment numbers. FAILURE OF YOUR ACKNOWLEDGMENT TO BE RECEIVED AT THE PLACE DESIGNATED FOR THE RECEIPT OF OFFERS PRIOR TO THE HOUR AND DATE SPECIFIED MAY RESULT IN

REJECTION OF YOUR OFFER. If by virtue of this amendment you desire to change an offer already submitted, such change may be made by telegram or letter, provided each telegram or letter makes reference to the solicitation and this amendment, and is received prior to the opening hour and date specified.

12. ACCOUNTING AND APPROPRIATION DATA (If required)

13. THIS ITEM APPLIES ONLY TO MODIFICATIONS OF CONTRACTS/ORDERS.

IT MODIFIES THE CONTRACT/ORDER NO. AS DESCRIBED IN ITEM 14.

A. THIS CHANGE ORDER IS ISSUED PURSUANT TO: (Specify authority) THE CHANGES SET FORTH IN ITEM 14 ARE MADE IN THE

CONTRACT ORDER NO. IN ITEM 10A.

B. THE ABOVE NUMBERED CONTRACT/ORDER IS MODIFIED TO REFLECT THE ADMINISTRATIVE CHANGES (such as changes in paying office, appropriation date, etc.) SET FORTH IN ITEM 14, PURSUANT TO THE AUTHORITY OF FAR 43.103(B).

C. THIS SUPPLEMENTAL AGREEMENT IS ENTERED INTO PURSUANT TO AUTHORITY OF:

D. OTHER (Specify type of modification and authority)

E. IMPORTANT: Contractor is not, is required to sign this document and return copies to the issuing office.

14. DESCRIPTION OF AMENDMENT/MODIFICATION (Organized by UCF section headings, including solicitation/contract subject matter where feasible.)

10A. MOD. OF CONTRACT/ORDER NO.

2. AMENDMENT/MODIFICATION NO.

5. PROJECT NO.(If applicable)

6. ISSUED BY

3. EFFECTIVE DATE

03-Jun-2020

CODE

W40M USA HLTH CONTRACTING ACT

REGIONAL HEALTH CONTRACT OFF CENTRAL

2539 GARDEN AVENUE

FT SAM HOUSTON TX 78234-0000

W81K00 7. ADMINISTERED BY (If other than item 6)

4. REQUISITION/PURCHASE REQ. NO.

CODE W81K00

FACILITY CODECODE

EMAIL:TEL:

SECTION SF 30 BLOCK 14 CONTINUATION PAGE

SUMMARY OF CHANGES

SECTION SF 30 - BLOCK 14 CONTINUATION PAGE

The following have been added by full text:

STATEMENT OF WORK UPDATED

HEMATOLOGY REAGENTS COST-PER-REPORTABLE

1. GENERAL REQUIREMENTS:

1.1. SCOPE OF WORK: The Contractor shall provide a cost-per-reportable arrangement for hematology testing reagents with the following incidental equipment: four (4) fully automated Hematology analyzer system in support of William Beaumont Army Medical Center, Fort Bliss, TX (inclusive of instruments, ancillary equipment, maintenance, services, repairs, support, and parts as required in order to maintain the systems in optimal operating condition, and any installation and removal). This will include the following three areas;

William Beaumont Army Medical Center Main Hospital, Soldier Family Medical Clinic, and Mendoza Clinic (SFCC). (See Para 5.1 for location). The cost for maintenance, reagents, consumables, and calibrators will be calculated into the cost of the kits. The Contractor shall perform to the standards of this contract.

1.2. QUALITY CONTROL (QC) and QUALITY ASSURANCE (QA):

1.2.1. The Contractor shall provide a Quality Control (QC) Plan (QCP) that contains, at a minimum, the items listed below to the Contracting Officer (KO) and Contracting Officer’s Representative (COR) for acceptance not later than 10 days AFTER the start of the contract. The KO will notify the Contractor of acceptance of required modifications to the plan. The Contractor shall make appropriate modifications and obtain acceptance of the plan by the KO.

1.2.1.1. The QC Plan shall include:

1.2.1.1.1. A description of the inspection system to cover all incidental support and maintenance services for Contractor-owned analyzers/equipment under this contract. Description shall include specifics as to the areas to be inspected on both a scheduled and unscheduled basis, frequency of inspections, and the title and organizational placement of the inspectors. Additionally, control procedures for any Government provided keys or lock combinations shall be included.

1.2.1.1.2. A description of the methods to be used for identifying and preventing equipment failure and/or defects.

1.2.1.1.3. A description of the records to be kept to document inspections and corrective or preventive actions taken. NOTE: The records of inspections shall be kept and made available to the government throughout the contract performance period and for the period after contract completion until final settlement of any claims, if any, under this contract.

1.2.2. Equipment Troubleshooting. When the government performs troubleshooting with the Contractor, the Contractor shall replace all reagents, calibrators, controls and any other materials used at no additional cost to the government in accordance with (IAW) Paragraphs 5.4.2.1 and 5.4.2.2. If kits are used out of WBAMC inventory they will be replaced at no cost to WBAMC.

1.3. HOURS OF OPERATION:

1.3.1. Normal Hours of Operation. WBAMC 24/7; 0700-1630 M-F Soldier Family and Mendoza

1.3.1.1. Holidays. Routine equipment servicing and reagent delivery will not be required on standard federal holidays. If an emergency arises, equipment servicing and reagent delivery will be provided in accordance with Section 5.4.3 of this Statement of Work (SOW).

1.3.2. The Contractor shall provide equipment maintenance service/direct customer service and support, 24 hours/7 days a week, to include hotline telephone service, and direct connect remote instrument diagnostic capability to assist operators in correcting equipment operation problems.

1.3.3. Legal Holidays. The following legal holidays will be observed by the Government:

New Year’s Day 1 January

Martin Luther King’s Birthday Third Monday in January

President’s Day Third Monday in February

Memorial Day Last Monday in May

Independence Day 4 July

Labor Day First Monday in September

Columbus Day Second Monday in October

Veteran’s Day 11 November

Thanksgiving Day Fourth Thursday in November

Christmas Day 25 December

NOTE: Any of the above holidays falling on a Saturday will be observed on the preceding Friday; holidays falling on a Sunday will be observed on the following Monday. Any holidays that are declared by Presidential Executive Order shall be observed in the same manner as the holidays listed above.

1.4. CONSERVATION OF UTILITIES. During maintenance, the Contractor shall make sure employees practice utilities conservation. The Contractor shall be responsible for operating under conditions that prevent the waste of utilities to include:

1.4.1. Lights shall be used only in areas where work is actually being performed.

1.4.2. Employees shall not adjust mechanical equipment controls for heating, ventilation, and air conditioning systems.

1.4.3. Water faucets or valves shall be turned off when not in use.

1.4.4. Environmental and Hazardous Materials Handling. If the disposal of any waste or byproduct of the analyzers cannot be safely dumped into each of the facility’s drain system, the Contractor must provide guidelines for safely disposing these wastes or byproducts in accordance with local and national guidelines.

1.5. RECORDS. The Contractor shall maintain all records necessary to comply with regulatory requirements and Food and Drug Administration (FDA) standards. The Contractor shall be responsible for creating, maintaining, and disposing of only those Government required records that are specifically cited in this SOW. If requested by the Government, the Contractor shall provide the original record or a reproducible copy of any such record within 5 working days of receipt of the request.

1.6. REMOVAL OF EQUIPMENT. The Contractor shall not remove any equipment from the Government work site without prior approval of the COR or his/her designated representative.

1.7. UPGRADE OF EQUIPMENT. Subject to mutual agreement between the Government and the Contractor, instrumentation may be upgraded within the specifications of the contract as new technology may become available. New equipment must meet the agreement for the original solicitation and does not obligate the government to any additional costs or testing menu items.

1.8. SPECIAL WORKING CONDITIONS. All equipment, parts, materials, and incidental services supplied by the Contractor shall conform to the applicable Safety and Health Standards as indicated in the current Code of Federal Regulations, Title 29, Chapter XVII, paragraph 1910, Occupational Safety Health Act of 1970.

1.9. CONTRACTOR PERSONNEL.

1.9.1. Contractor Employees. The Contractor shall not employ persons for work on this contract if such employee is identified to the Contractor by the KO as a potential threat to the health, safety, security, general well-being or operational mission of the installations and their population.

1.9.1.1. Contractor employees shall present a neat appearance and be easily recognized as Contractor employees. Contractor personnel shall either wear a distinguishable uniform or badge on the exterior of their clothing while performing any service at any government facility.

1.9.1.2. The Contractor shall not employ any person who is an employee of the US government. Additionally, the Contractor shall not employ any person who is an employee of the Department of Defense (DoD), either military or civilian, unless such person seeks and receives approval according to DOD 5500.7R, “Joint Ethics Regulation”. The Contractor shall not employ any person who is an employee of the Department of Defense, if such employment would be contrary to local policies.

1.9.1.3. The Contractor employees will be registered with the Symplr© system for WBAMC. Contractors must check in with Symplr© and report to PMO to check in. At no time is the Contractor employee to walk about the WBAMC without an escort. PMO will contact the COR to escort the contractor to the laboratory area.

1.9.1.4 Contractor employees will not be admitted to the Department of Pathology without a prior scheduled appointment. No walk-ons will be accepted by the COR.

2. DEFINITIONS/ACRONYMS.

2.1. DEFINITIONS. Following is a list of basic definitions.

2.1.1. CONTRACTING OFFICER (KO): The ONLY person with the authority to enter into, administer, change, and/or terminate contracts and make related determinations and findings.

2.1.2. CONTRACTING OFFICER'S REPRESENTATIVE (COR): A government employee selected and designated in writing by the Contracting Officer to act as his/her designated representative in administering a contract. NOTE: The COR is not authorized to make any changes to the terms and conditions of the contract.

2.1.3. QUALITY ASSESSMENT AND IMPROVEMENT. Those actions taken by the Government to check services to determine if they meet the requirements of the CLIA/DoD CLIP ’88 & ’03, CAP, JCAHO, U.S. Army Medical Command and U.S. Navy Bureau of Medicine quality assurance and risk management programs, and ensure compliance with the terms and conditions of the contract

2.1.4. QUALITY CONTROL. Those actions taken by a Contractor to control the performance of services to ensure that they meet the requirements of the contract.

2.1.5. SERVICES: Includes incidental maintenance services and support performed and materials furnished or utilized to maintain the equipment.

2.1.6. QUALITY IMPROVEMENT (QI): Those actions taken by the Government, in accordance with WBAMC DPALS Quality Plan, relevant CSLI standards for quality, AR 40-68, to assure services meet the requirements of the contract.

2.2. ACRONYMS/ABBREVIATIONS. Following is a list of basic acronyms/abbreviations used in the contract.

AR - Army Regulation BUMED - U.S. Navy Bureau of Medicine and Surgery CAP - College of American Pathologists DA - Department of the Army DN - Department of the Navy DoD CLIP - Department of Defense Clinical Laboratory Improvement Program HIPAA - Health Insurance Portability & Accountability Act of 1996 MAS Minimum Acceptable Standards MEDCOM - U.S. Army Medical Command TJC - The Joint Commission OSHA - Occupational Safety and Health Administration PMS Preventive Maintenance Services

PRS Performance Requirements Summary QA - Quality Assurance QA&I - Quality Assessment & Improvement QC - Quality Control WBAMC William Beaumont Army Medical Center

3. GOVERNMENT-FURNISHED FACILITIES, EQUIPMENT, MATERIAL, AND SERVICES. The Government will provide, without additional cost to the Contractor, the facilities, equipment, materials, and services listed below.

3.1. FACILITIES. The government will furnish the facilities for set-up and operation of the Contractor equipment analyzers required in support this contract. The Contractor shall not alter the facilities without written approval of the KO. The Contractor shall return the facilities to the government in the same condition as received, fair wear and tear and approved modifications excepted. These facilities shall be used for performance of this contract only.

3.2. EQUIPMENT.

3.2.1. Contractor will supply at a minimum (2) two Automated Hematology analyzers for William Beaumont Army Medical Center, new hospital location. If the minimum required analyzers are not enough to meet the workload demands the Contractor, an additional Hematology analyzer shall be supplied by the Contractor. The contractor shall also provide (1) one Automated Hematology analyzer for the Mendoza Clinic (SFCC), FT Bliss and (1) one Automated Hematology analyzer for Soldier Family Medical Center (SFMC), FT Bliss.

3.3. SERVICES. The government will provide the following services at no cost to the Contractor:

3.3.1. The government will provide the normal range of facility utilities (e.g. electricity, water, heating, refuse collection, etc.) and other utilities necessary for the full functionality of the equipment/instrumentation.

3.3.2. Security: Police and Fire Protection, as is provided other personnel.

3.3.3. Emergency Healthcare for Contractor employees. The MTF will provide emergency healthcare for injuries or life threatening medical emergencies occurring while on duty. The Contractor shall reimburse the government for such services as billed by the MTF, unless the Contractor employee is otherwise authorized to receive such services at no cost (e.g., is retired military or is a military dependent).

4. CONTRACTOR FURNISHED PROPERTY

4.1. General. Except for those government-furnished items and services specified in section 3, the Contractor shall furnish all items, equipment, and incidental support and maintenance services required under this contract.

4.2. Transportation. Transportation in support of any equipment and incidental support and maintenance services is the responsibility of the Contractor. The government will not provide transportation.

4.3. Nametags. The Contractor shall furnish a nametag for each contract employee. The nametag shall contain the name of the company and the employee and must be worn at all times when at the government’s facilities.

5. SPECIFIC TASKS

5.1. DESCRIPTION

5.1.1. The Contractor shall provide a two (2) fully automated hematology systems capable of performing all of the required assays listed in Appendix 1 through continuous random access operations and the ability to connect to the laboratory information system bi-directionally through middleware platform. The systems shall provide redundancy (to ensure continuous operations). Contractor shall provide training, supplies, reagents, unscheduled and preventative maintenance in accordance with OEM standards. Contractor shall include delivery, installation, all calibrators/standards, reagents/reagent packs, and quality control materials necessary to perform the specified assays, initial method validations per CLIA/NCCLS/DPALS QM guidelines and analyzer removal upon termination of the contract. All costs shall be calculated on a cost per reportable based on the number of patients listed at Appendix 1. Costs shall be amortized over the total number of test and factored into the cost per test.

5.1.1.1. For the purposes of this SOW the analyzer system includes at a minimum:

- All analyzers

- Peripherals (e.g. instrument specific computer terminals and CPUs, printers, etc.)

- Middleware

- Uninterruptable Power Sources (UPS)

5.1.1.2. The analyzer systems and main line will be located at:

William Beaumont Army Medical Center 18511 Charlie Medic Way

El Paso, TX 799218

5.1.1.2.1 Validation/Correlation of equipment at WBAMC will require a minimum 60 days. Equipment must be installed at the new hospital location 60 days prior to October 1, 2020. Validation, correlation, and training must be completed by September 27, 2020.

5.1.1.3. The contractor shall provide automated hematological analysis capabilities to SFMC and SFCC. Each facility will be given a single, desktop analyzer in order to meet space restrictions. The analyzers must be capable of performing all of the required assays listed in Appendix 1 for each area. Contractor shall include delivery, installation, all calibrators/standards, reagents/reagent packs, and quality control materials necessary to perform the specified assays, initial Method Validations per CLIA/NCCLS/DPALS QM guidelines and analyzer removal at the termination of the contract.

5.1.1.3.1. The analyzer systems will be located at:

Soldiers Family Medical Clinic (SFMC) 2496 Wicker Rd.

Ft. Bliss, TX 79916

Mendoza Clinic (SFCC) 11335 SSG Sims St.

East Ft. Bliss, TX 79916

5.1.1.3.2. Validation/Correlation of equipment for the clinics will require a minimum 60 days. Equipment must be onsite 60 days prior to October 1, 2020. Validation, correlation, and training must be completed by September 27, 2020.

5.1.2. Within 10 working days after contract award, Contractor shall coordinate and conduct a post-award site visit for the purpose of coordinating schedule for equipment installation. The Laboratory is undergoing complete renovations so this is critical to ensure electrical, drainage, etc. needs are identified early. Additionally, the installation of equipment may need to be performed in a phase process at no additional cost to the government.

5.1.3. Method validation will be at no cost to the government. All reagents, consumables, calibrators, and QC required to complete the validation will be covered by the Contractor. The Contractor will only be paid once validation is complete and patients are being run.

5.1.3.1. Method validation shall be conducted IAW method validation protocols established by the Department of Pathology’s Quality Management Program (these protocols are IAW applicable standards as described by the Clinical Laboratory Standards Institute (CLSI) and/or required by the College of American Pathologists (CAP)). Relevant guidelines listed in Appendix 2 (below) are the minimum guidelines that will be referenced when conducting method validation. Additional guidelines may be required, depending on regulatory requirements.

5.1.3.2. Method validation shall include, but not be limited to, reference range verification, demonstration of linearity with limit of quantitation verification (LOQ), limit of detection verification (LOD), reportable range, correlation with current methods (comparison of methods study), validation of analytical measurement range (AMR), validation of clinical reportable range (CRR), validation of imprecision (within day and between day) and accuracy (recovery study), and establishment of initial control ranges using control materials, to include third party controls, as designated by the Laboratory Director.

5.1.3.3. The Contractor shall provide a qualified Technical Service Representative on site for the duration of the validation/verification time frame at no additional cost to the government. The technical service representative must possess a thorough knowledge of method validation and is familiar with the use of statistical evaluation software as determined by the Laboratory Director (e.g. EP Evaluator®), to provide technical assistance for the method validation studies. The assigned Technical Service Representative will be responsible for the entire method validation.

5.1.3.4. The Government’s Technical Supervisor will obtain patient specimens for use in the Method Validation.

In the event that specimen requirements for correlation studies cannot be met (e.g., insufficient number of patients to challenge the extremes of a curve), the Contractor shall assist in procuring additional specimens. These specimens may be obtained from other laboratories or from Contractor sources, but will be at no cost to the government.

5.1.3.5. If an appropriate number of patient samples cannot be procured to meet the Medical Director’s approval validation of those identified tests may be discontinued until a later time. The Contractor will be contacted when the facility is ready to validate the test and the Technical Service Representative will return onsite to complete the validation at no cost to the government.

5.1.3.6. Both the Contractor and Contractor personnel at each location shall abide by all Health Insurance Portability & Accountability Act of 1996 (HIPAA) rules and regulations when conducting the Method Validation Study.

5.1.4. The Contractor shall provide two (2) paper and two (2) CD copies of the operator’s and maintenance manuals and a statement of the warranty terms in the English language. The level of detail required of appropriate instrument maintenance manuals extends only to routine maintenance procedures performed by the user.

5.1.5. The Contractor shall provide material safety data sheets (MSDS) for each item delivered under this contract that is considered to be HAZARDOUS MATERIAL by the United States or the Contractor’s representative government. The MSDS shall contain information on the hazards associated with each specific chemical or material. The MSDS shall be printed in the English language and shall contain, as a minimum, identification of:

- The hazardous material

- The specific hazard

- The required practices for the safe use of the product

- First aid procedures

- What to do in the event of a spill or other mishap or accident.

5.1.6. The Contractor shall provide the reagents and shall coordinate exact quantities and shipment schedule with the COR prior to shipment IAW Paragraph 5.3.14, Deliveries.

5.1.7. The Contractor shall collect and transport equipment upon termination of this contract.

*** 5.2. HEMATOLOGY ANALYZERS: WBAMC Main Hospital Laboratory. The contractor shall provide, at a minimum, two (2) fully automated, bi-directional hematology analyzers with: 1) advanced cytometry imaging technique/methodology; 2) “Microtainer” micro-sample capability; 3) minimal significant effects from interfering substances; 4) Use of single aspiration needle for both open and close mode sampling. The total number of analyzers shall be determined by the minimum throughput, available menu requirements, patient acuity and be able to continually operate for 12-hrs without having to stop to load reagents or consumables. See equipment minimum requirements paragraph 3.2 Equipment.

5.2.1. Minimum actual through-put shall be: 1) up to 100 Whole Blood Complete Blood Cell Counts (CBC) with differential and Reticulocytes counts per hour; 2) Nucleated Red Blood Cell Analysis – Capable of performing automatic NRBC differential and automatic correction of the white blood cell count. Be able to provide Quality Control material for NRBCs as well.

5.2.2. Each analyzer shall be a continuous random access analyzer system with STAT prioritization capability and a closed primary tube sampling system capable of cap-piercing and be capable of loading at least 25 STAT samples at a time.

5.2.3. Be able to recognize LIS generated bar-code labels (both code 39 and 128) on primary sample tubes.

*** 5.2.4. Using advanced cytometry imaging technique/methodology is capable of determining platelet clumping, enlarged platelets, hypo or hyper-granulated platelets, and can differentiate between a large platelet and small red blood cell without a manual differential to confirm.

*** 5.2.5. Using advanced cytometry imaging technique/methodology is capable of performing body fluids cell count to include the following specimens, cerebrospinal fluid (CSF), synovial fluids and serous fluids.

Report will include Total Nucleated Cell (TNC) and total Red Blood Cells and two part differential (MN and PMN). Be able to provide Quality Control materials as well.

5.2.6. Ability to interconnect multiple analyzers as one and used simultaneously as independent analyzers.

Allows the connection of a slide maker and a slide stainer and an automated digital cell morphology analyzer/software.

5.2.7. Specimen Storage: The analyzer needs to be able to analyze samples with limited flags or failures under the following conditions. For CBC/Diff, samples stored at room temperature for up to 24 hrs or refrigerated (2-8 C) for up to 48 hrs. For reticulocytes, room temperature for up to 24 hrs and refrigerated for up to 72 hrs. For nucleated red blood cells, room temperature or refrigerated up to 24 hrs.

5.2.8. All analyzer/data management system displays and supporting literature shall be in the English language.

5.2.9 Initial startup from the shutdown state shall (must) not exceed 20 minutes.

5.2.10 Each analyzer system must come equipped with an un-interruptible power supply (UPS) capable of providing all necessary electrical power to each analyzer system for 15 to 20 minutes. The Contractor is responsible to ensure the UPS remains maintained and operable throughout the length of the contract. The power cord for the UPS must be a minimum of 11 foot in length for the WBAMC Main Hospital due to overhead ceilings outlets.

5.2.11 Data Management system shall (must) have a user friendly "Windows Based" interface that shall include a data management system for operational control of the analyzer system, management of the QC program, on- instrument useful life of the reagents/reagent packs, and management of patient results.

5.2.12 The software shall provide a single operator interface for workload management, data management, and instrument operational status monitoring. The software controls the operations of the analyzer, monitors the lot number expiration date of on-board reagents and control materials. This shall be accomplished via communication connections between the automation, analyzers, and hospital Laboratory Information System (LIS).

5.2.13 The results management application shall manage patient data, sample and QC results by offering archiving, status, calculation of results and long-term results storage.

5.2.14 The software shall provide proactive monitoring of key instrument parameters to allow for predictive diagnostics.

5.2.15 The Contractor shall provide a Thin Client-type data management system that allows for remote operational control of the analyzer system, management of the quality control program, on-instrument useful life of the reagents/reagent packs, and management of patient results.

5.2.16 The Thin Client shall provide a dynamic display sample status, allow for dynamic/real-time review and management of the quality control program, review of on-instrument useful life of the reagents/reagent packs, and management of patient results instrument. In addition, the status of automation components and communications shall be able to be monitored from a single remote interface.

5.2.17 The Thin Client shall provide a dynamic interface with other analyzers that are not physically attached to the automation line. These analyzers may, or may not be from the same vendor. This interface at a minimum shall provide information as to the presence of specimens on the analyzer, and may act as a conduit for results management.

5.2.18 Remote diagnostics and troubleshooting shall be available using a maintenance application program that allows technical and service specialists at the Contractors technical support center or a field representative to remotely access the instruments to diagnose a problem.

5.2.19 The Contractor shall provide a middleware solution and full IT support as defined below at no addition cost to the Government throughout the life of the contract. Middleware capabilities shall include, at a minimum, the following features:

5.2.20 The capability to write user defined auto-verification/auto-result validation rules that can hold transmission of results for review by the user.

5.2.21 The capability to validate user defined auto-verification/result validation rules.

5.2.22 Support patient delta checks as part of the auto-verification process.

5.2.23 Establish Moving Averages (Average of Normals) protocols to identify trends that may affect patient results.

5.2.24 Store patient results for a minimum of 12-months to facilitate auto-verification/auto-result.

5.2.25 The analyzer systems and all reagents shall be approved by the Food & Drug Administration (FDA).

All analyzers and associated parts and accessories shall be new. No used, refurbished, or like-new equipment shall be provided in support of this contract at any time.

5.2.26 The Contractor shall provide consumables, reagent containers, etc. in sufficient quantities and quality to perform these assays.

*** 5.2.27. HEMATOLOGY ANALYZERS (Mendoza and Soldier Family) - - The contractor shall provide

One (1) each standalone CBC analyzer capable of performing a full test profile (CBC with multi-part differential to include at least: neutrophils, lymphocytes, monocytes, eosinophils, basophils and immature white blood cells, fluorescent NRBC count) using 88 ul of sample. Must include a pre-diluted sample access mode for lower sample volume of 70 ul to perform full hematology test profile.

5.2.28 Platelet counts must be able to read down to zero and verified on file.

*** 5.2.29. All tests must have FDA approval. Must have white blood cells detection capability. These tests must include reportable immature white blood cells absolute values and percentages as part of the multi-part differential to include at least: neutrophils, lymphocytes, monocytes, eosinophils, basophils and immature white blood cells.

5.2.30 Able to process without operator intervention once the run time has started: 100% walk-away.

Instrument must have above 95% uptime, with a 5% or less downtime per year. Contractor shall provide information to support this requirement.

5.2.31 Must have a single aspiration pathway for open and closed tube sampling to eliminate the need for mode to mode correlation.

5.2.32 Must be capable of achieving WBC linearity range of 0.0-440.0 x10^3/ul and directly measure HCT with a linearity and reportable range of 0.0-75.0%.

5.2.33 Daily shutdown and initial startup time shall not exceed 20 minutes.

5.2.34 Space limitations: 30” x 42.

5.2.35 Minimum actual through-put shall be: 1) up to 100 Whole Blood Cell (WBC) counts with differential and Reticulocytes counts per hour; 2) Nucleated Red Blood Cell Analysis – Capable of performing automatic NRBC differential and automatic correction of the white blood cell count. Be able to provide Quality Control material for NRBCs as well.

5.2.36 Each analyzer shall be a continuous random access analyzer system with STAT prioritization capability and a closed primary tube sampling system capable of cap-piercing and be capable of loading at least 25 STAT samples at a time.

5.2.37 Be able to recognize LIS generated bar-code labels (both code 39 and 128) on primary sample tubes.

*** 5.2.38. Using advanced cytometry imaging technique/methodology is capable of determining platelet clumping, enlarged platelets, hypo or hyper-granulated platelets, and can differentiate between a large platelet and small red blood cell without a manual differential to confirm.

*** 5.2.39. Using advanced cytometry imaging technique/methodology is capable of performing body fluids cell count to include the following specimens, cerebrospinal fluid (CSF), synovial fluids and serous fluids. Report will include Total Nucleated Cell (TNC) and total Red Blood Cells and two part differential (MN and PMN). Be able to provide Quality Control materials as well.

5.2.40 Specimen Storage: The analyzer needs to be able to analyze samples with limited flags or failures under the following conditions. For CBC/Diff, samples stored at room temperature for up to 24 hrs or refrigerated (2-8 C) for up to 48 hrs. For reticulocytes, room temperature for up to 24 hrs and refrigerated for up to 72 hrs. For nucleated red blood cells, room temperature or refrigerated up to 24 hrs.

5.2.41 All analyzer/data management system displays and supporting literature shall be in the English language.

5.2.42 Data Management system shall (must) have a user friendly "Windows Based" interface that shall include a data management system for operational control of the analyzer system, management of the QC program, on- instrument useful life of the reagents/reagent packs, and management of patient results.

5.2.43 The software shall provide a single operator interface for workload management, data management, and instrument operational status monitoring. The software controls the operations of the analyzer, monitors the lot number expiration date of on-board reagents and control materials. This shall be accomplished via communication connections between the automation, analyzers, and hospital Laboratory Information System (LIS).

5.2.44 The software shall provide proactive monitoring of key instrument parameters to allow for predictive diagnostics. The results management application shall manage patient data, sample and QC results by offering archiving, status, calculation of results and long-term results storage.

5.2.45 The Contractor shall provide a Thin Client-type data management system that allows for remote operational control of the analyzer system, management of the quality control program, on-instrument useful life of the reagents/reagent packs, and management of patient results.

5.2.46 The Thin Client shall provide a dynamic interface with other analyzers that are not physically attached to the automation line. These analyzers may, or may not be from the same vendor. This interface at a minimum shall provide information as to the presence of specimens on the analyzer, and may act as a conduit for results management.

5.2.47 Remote diagnostics and troubleshooting shall be available using a maintenance application program that allows technical and service specialists at the Contractors technical support center or a field representative to remotely access the instruments to diagnose a problem.

5.2.48 The Contractor will provide a middleware solution and full IT support as defined below at no addition cost to the Government throughout the life of the contract. Middleware capabilities shall include, at a minimum, the following features:

5.2.49 The capability to write user defined auto-verification/auto-result validation rules that can hold transmission of results for review by the user.

5.2.50 The capability to validate user defined auto-verification/result validation rules.

5.2.51 Support patient delta checks as part of the auto-verification process.

5.2.52 Establish Moving Averages (Average of Normals) protocols to identify trends that may affect patient results.

5.2.53 Store patient results for a minimum of 12-months to facilitate auto-verification/auto-result.

5.2.54 The analyzer systems and all reagents shall be approved by the Food & Drug Administration (FDA).

All analyzers and associated parts and accessories shall be new. No used, refurbished, or like-new equipment shall be provided in support of this contract at any time.

5.2.55 The Contractor shall provide consumables, reagent containers, etc. in sufficient quantities and quality to perform these assays.

5.3. REAGENTS.

5.3.1. The analyzer shall have the on-board ability to maintain reagents at the proper storage temperatures for the assays listed in Appendix 1. All assays must be FDA approved.

5.3.2. The workload listed in Appendix 1 is an estimate based on projected patient workload. Actual workload may vary. The workload numbers represent patient reportable results, and do not include calibrators, controls, or re- runs due troubleshooting or specimen dilutions.

5.3.3. The actual workload may fluctuate in the first year of the contract due to changes in the distribution of patient care. In addition, workload may expand in subsequent option years due to fluctuations in patient volume, and with the inclusion of other locations. Appendix 1 provides the estimated workload for Contract Year 1 as well as an estimated workload for each option year. All workload numbers represent total estimated patient reportable results for the indicated year.

5.3.4. The analyzer shall be capable of maintaining calibration curves for all of the assays listed in Appendix 1 simultaneously.

5.3.5. The assays listed in Appendix 1 shall must be present on the analyzer at all times.

5.3.6. Reagents shall must have a minimum shelf life of three (3) months upon receipt by the Government, or, if this shelf life requirement cannot be met, the Contractor shall (must) identify the guaranteed shelf life after receipt that can be accommodated in their response to the Request for Proposal.

5.3.7. Controls will have shelf life of 4-12 weeks.

5.3.8. An alternate quality control material must be provided by the contractor if the new lot of controls cannot be delivered two weeks prior to the expiration date of the lot currently in use.

5.3.9. All test kits will be provided as follows:

5.3.9.1. Inclusive of an English language package inserts.

5.3.9.2. Be provided by the manufacturer of the equipment.

5.3.9.3. Delivered on time, at the appropriate storage temperature, and marked with any required temperature controls as necessary.

5.3.9.3.1. Routine or scheduled orders will arrive within one week before or after the scheduled date of delivery.

5.3.9.3.2. Emergency orders will be delivered within 24 hours after the order is placed.

5.3.9.4. Be compatible with all reagent packs used with the Analyzers.

5.3.9.5. Preservation and packing - preservation and packing shall be performed in accordance with the best commercial practice and in such a manner to afford adequate protection against any damage during shipment from source to destination.

5.3.9.6. The Contractor shall provide the reagents as outlined in the Schedule of Supplies/Services.

Delivery of the reagents will be as scheduled/required by the individual delivery orders issued by the contracting officer.

5.3.9.7. The Contractor shall provide an estimate of the yearly quantities of reagent/reagent packs, calibrators/standards, and quality control materials required to perform the volume of patient reportable tests for each assay as provided in Appendix 1.

5.3.9.8. The Contractor shall provide quality control materials sufficient to run every 8-hours and to be used as needed for troubleshooting. This includes third-party controls where requested/required by the laboratory. These controls and calibrators should be at no cost to the government.

5.3.9.9. The Contractor shall pre-program and adjust program as necessary for all quality control, maintenance, calibrator material in vendor provided racks or testing containers.

5.3.9.10. The Contractor shall ensure that requirements for routine quality control runs (as defined by the Laboratory Director and outlined in the Laboratory QA program), routine calibration, periodic calibration/calibration verification (i.e., each assay must be calibrated or have calibration verification performed at intervals not to exceed a 6-month period of time), specimen dilutions, and for troubleshooting of out-of-control assays be considered when calculating the yearly requirements.

5.3.9.11. The Contractor shall estimate the volume of user-replaceable maintenance items that will be required to support the analyzer, and any analyzer specific tools/supplies necessary to perform operator-level periodic maintenance tasks, at the level of use specified in Appendix 1. An operator level maintenance tool/ parts kit will be provided and replenishment of all expended items will be made by the contractor, at no additional cost to the Government. Replenishment shall be made as needed or on a periodic basis not to exceed the normal preventive maintenance cycle.

5.3.10. Calibration frequency for all assays shall not be less than twice a year (every 6 months) under routine operations. This calibration frequency does not include calibrations required following instrument repair or servicing (e.g., field service type maintenance or service, major changed in instrument components that affect readout, QC troubleshooting, etc.) or other instances as described in the Laboratory QA Program or approved by the Laboratory Director.

5.3.10.1 All reagents provided shall be identical to those used in the FDA 510K approval application.

All reagents/reagent packs shall be provided as follows:

5.3.10.2 Be provided by the manufacturer of the equipment.

5.3.10.3 Be marked with the required storage temperature.

5.3.10.4 Be maintained at the proper storage temperature during transportation from the Contractor’s storage facility to the Government acceptance site and be delivered on time at the appropriate storage temperature.

5.3.11 The Contractor shall provide the reagents/reagents packs, calibrators/standards, quality control materials, user-replaceable maintenance items, and analyzer specific tools/supplies as outlined in the Schedule of Supplies/Services.

5.3.12. The Contractor shall provide linearity materials for all testing that spans the vendor’s published analytical measuring range (AMR) every six-months and as needed to verify repairs per the College of American Pathologist (CAP) inspection criteria.

5.3.13. Deliveries.

5.3.14. Deliveries of required items shall be per monthly standing orders as agreed upon between the Contractor and the Government. The Contractor needs to specify the last date that a standing order can be modified for a single delivery and/or all subsequent orders. Orders shall arrive on the date agreed upon and if the scheduled date is a Federal Holiday (listed above), the delivery will be scheduled for the day following the Federal Holiday. Any supplies that are placed on back order shall be clearly identified on the shipping documents and shall be delivered in a timely manner, not to exceed ten (10) working days. In the instance a back-order exceeds 10 working days, the Contractor shall provide testing services through local sub-contract at their cost.

5.3.14.1. Emergency orders shall be delivered within 24 hours after the order is placed and be of the same lot number of calibrators/standards, reagents/reagent packs, or quality control materials currently in use for the assay(s) for which supplies are being requested. Contractor will notify the Government via email and telephonic message when an order is not available or capable to be shipped within these timelines.

5.3.14.2. For all orders, standing or emergency, the Contractor shall notify via email the designated points of contact that orders have shipped and provide a tracking number.

5.3.14.3 Preservation and packing - Preservation and packing shall be performed in accordance with the best commercial practice and in such a manner to afford adequate protection against any damage during shipment from source to destination. All packaging and shipping information shall be clearly marked as to contents on both the shipping documents and the shipping container/box. All deliveries will be made Tuesday through Thursday, to exclude Federal Holidays.

5.4. ANCILLARY MAINTENANCE AND SERVICE

5.4.1. ANCILLARY MAINTENANCE. The Contractor shall be responsible for furnishing maintenance, services, repairs, and parts as required in order to maintain the systems in optimal operating condition.

5.4.1.1. The Contractor shall maintain all equipment installed under this contract except for repairs necessitated by willful damage or negligence on the part of the Government.

5.4.1.2. The Contractor shall provide all personnel, equipment, tools, materials, supervision, parts, transportation, and other items and services necessary to perform all required repairs and scheduled preventive maintenance/safety inspections and calibrations of equipment. The performance of scheduled periodic preventive maintenance, safety checks, and calibrations that are not normally performed at the operator level shall be performed by Contractor service personnel in accordance with requirements as specified in the Contractor’s instrument maintenance manual. Completion of installation of the analyzers will establish time zero for determination of time frames for performance of the above periodic services.

5.4.1.3. The Contractor shall provide a full unscheduled and preventive maintenance service for the lease period at no additional cost. Service shall include repair and replacement of defective parts, complete maintenance program (as required by the manufacturer’s maintenance manuals), and hotline telephone service, to assist operators in troubleshooting problems in accordance with paragraph 5.4.3.1. of this SOW.

5.4.2. REPAIR. Upon notification of equipment failure, the Contractor’s qualified service technician shall establish telephonic contact within 60 minutes of the Government notification to the Contractors Customer Service “Hotline” and shall be on-site to provide unlimited emergency service (service requiring immediate repair) within four (4) hours of establishing telephonic contact. The equipment shall be repaired and operational within 48 hours after initial response by the Contractor. Should both instruments become inoperable, the Contractor’s technical specialist must be on-site within four (4) hours of initial notification. If the equipment cannot be repaired, a replacement instrument shall be provided within 72 hours. The Contractor shall provide replacement parts as necessary for operator level maintenance.

5.4.2.1. The Contractor shall provide all reagents, calibrators, controls and any other materials necessary to troubleshoot the reasons for the analyzer failure at no additional cost.

5.4.2.2. The Contractor shall replace all reagents, calibrators, controls and any other materials used by the Government to trouble shoot the instrument failure prior to notification of the contractor.

5.4.2.3. All work shall be performed in a professional manner by an authorized service representative. If any deficiencies are found due to negligence of the service representative, the Contractor shall be required to correct the deficiency to a fully operational status in accordance with manufacturer specifications at no additional cost to the Government.

5.4.2.3. All correspondence, service reports, and invoicing shall be in English.

5.4.2.4. Preventive maintenance services shall be performed in accordance with the manufacturer’s standards/procedures. A preventive maintenance service shall include, but is not limited to, safety, calibration, complete operational testing, lubrication, adjustments, and cleaning of equipment to which the operator does not have access. This also includes the installation of all non-operator parts required to ensure proper operation.

5.4.2.4.1. The Contractor shall notify the COR or ACOR of the exact date and time for performance of a preventive maintenance service within ten (10) days prior to the scheduled preventive maintenance services.

5.4.2.5. The use of two-way radios, as well as smoking, is prohibited within WBAMC and outlying clinics.

5.4.2.6. Prior to performing Scheduled Maintenance and Unscheduled Repair Services work, the Contractor's representative shall report to and obtain from the Equipment Management Branch, at the MTF a Visitors Badge. The badge must be returned to the Equipment Management Branch prior to departing the MTF.

5.4.2.7. Within 2 business days after completion of a repair, the Contractor’s representative shall furnish via email the COR one (1) copy of a service report for all services performed with a copy to the Equipment

Management Branch and the Laboratory Representative for the MTF. The report shall be in English and shall contain, as a minimum, the following information:

Nomenclature and serial number Date Description of services performed (i.e., preventive maintenance service, or unscheduled repair service) Location of services performed Duration of performance (hours) List of parts…