36C25724Q0485.pdf

PAGE 1 OF 1. REQUISITION NO.

2. CONTRACT NO. 3. AWARD/EFFECTIVE DATE 4. ORDER NO. 5. SOLICITATION NUMBER 6. SOLICITATION ISSUE DATE

a. NAME b. TELEPHONE NO. (No Collect Calls) 8. OFFER DUE DATE/LOCAL

TIME

9. ISSUED BY CODE 10. THIS ACQUISITION IS UNRESTRICTED OR SET ASIDE: % FOR:

SMALL BUSINESS

HUBZONE SMALL

BUSINESS

SERVICE-DISABLED

VETERAN-OWNED

SMALL BUSINESS

WOMEN-OWNED SMALL BUSINESS

(WOSB) ELIGIBLE UNDER THE WOMEN-OWNED

SMALL BUSINESS PROGRAM

EDWOSB

8(A)

NAICS:

SIZE STANDARD:

11. DELIVERY FOR FOB DESTINA-

TION UNLESS BLOCK IS

MARKED

SEE SCHEDULE

12. DISCOUNT TERMS

13a. THIS CONTRACT IS A

RATED ORDER UNDER

DPAS (15 CFR 700)

13b. RATING

14. METHOD OF SOLICITATION

RFQ IFB RFP

15. DELIVER TO CODE 16. ADMINISTERED BY CODE

17a. CONTRACTOR/OFFEROR CODE FACILITY CODE 18a. PAYMENT WILL BE MADE BY CODE

TELEPHONE NO. UEI: EFT:

PHONE: FAX:

17b. CHECK IF REMITTANCE IS DIFFERENT AND PUT SUCH ADDRESS IN OFFER

18b. SUBMIT INVOICES TO ADDRESS SHOWN IN BLOCK 18a UNLESS BLOCK BELOW IS CHECKED

SEE ADDENDUM

19. 20. 21. 22. 23. 24.

ITEM NO. SCHEDULE OF SUPPLIES/SERVICES QUANTITY UNIT UNIT PRICE AMOUNT

(Use Reverse and/or Attach Additional Sheets as Necessary)

25. ACCOUNTING AND APPROPRIATION DATA 26. TOTAL AWARD AMOUNT (For Govt. Use Only)

27a. SOLICITATION INCORPORATES BY REFERENCE FAR 52.212-1, 52.212-4. FAR 52.212-3 AND 52.212-5 ARE ATTACHED. ADDENDA ARE ARE NOT ATTACHED.

27b. CONTRACT/PURCHASE ORDER INCORPORATES BY REFERENCE FAR 52.212-4. FAR 52.212-5 IS ATTACHED. ADDENDA ARE ARE NOT ATTACHED

28. CONTRACTOR IS REQUIRED TO SIGN THIS DOCUMENT AND RETURN _______________ 29. AWARD OF CONTRACT: REF. ___________________________________ OFFER COPIES TO ISSUING OFFICE. CONTRACTOR AGREES TO FURNISH AND DATED ________________________________. YOUR OFFER ON SOLICITATION DELIVER ALL ITEMS SET FORTH OR OTHERWISE IDENTIFIED ABOVE AND ON ANY (BLOCK 5), INCLUDING ANY ADDITIONS OR CHANGES WHICH ARE ADDITIONAL SHEETS SUBJECT TO THE TERMS AND CONDITIONS SPECIFIED SET FORTH HEREIN IS ACCEPTED AS TO ITEMS:

30a. SIGNATURE OF OFFEROR/CONTRACTOR 31a. UNITED STATES OF AMERICA (SIGNATURE OF CONTRACTING OFFICER)

30b. NAME AND TITLE OF SIGNER (TYPE OR PRINT) 30c. DATE SIGNED 31b. NAME OF CONTRACTING OFFICER (TYPE OR PRINT) 31c. DATE SIGNED

AUTHORIZED FOR LOCAL REPRODUCTION (REV. NOV 2021)

PREVIOUS EDITION IS NOT USABLE Prescribed by GSA - FAR (48 CFR) 53.212

7. FOR SOLICITATION

INFORMATION CALL:

STANDARD FORM 1449

SOLICITATION/CONTRACT/ORDER FOR COMMERCIAL PRODUCTS AND COMMERCIAL SERVICES

OFFEROR TO COMPLETE BLOCKS 12, 17, 23, 24, & 30

36C25724Q0485 04-01-2024

Ivan Torres ivan.torres1@va.gov 04-08-2024 10:00am CST

36C257 Department of Veterans Affairs NCO 17 North Texas Healthcare System Regional Procurement Office West (RPO-W) 5441 Babcock Rd. Ste.302 San Antonio TX 78240

X 100

X

541690

$19 Million

N/A

X

36C257

Department of Veterans Affairs Audie Murphy VA Medical Center

SOUTH TEXAS VAHCS

7400 Merton Minter Boulevard San Antonio TX 78229

36C257

Same as block 9.

This is accomplished through the Tungsten Network located at:

http://www.fsc.va.gov/einvoice.asp This is mandatory and the sole method for submitting invoices.

(877) 353-9791 (512) 460-5540

See CONTINUATION Page

The contractor shall provide Diagnostic Medical Physics Services.

For additional details reference the Price/Cost Schedule and

SOW Statement of Work.

NOTIFICATION TO OFFEROR:

Offerors must complete and return all information required by this solicitation prior to the time specified in block B of SF 1449 (Page 1)

SF 1449: Block 30a, 30b and 30c must be complete and signed in order to be considered for award.

x X x 1

Astrid McKinney Contracting Officer

36C25724Q0485

Table of Contents

SECTION A

A.1 SF 1449 SOLICITATION/CONTRACT/ORDER FOR COMMERCIAL PRODUCTS

AND COMMERCIAL SERVICES

SECTION B - CONTINUATION OF SF 1449 BLOCKS

B.1 CONTRACT ADMINISTRATION DATA

B.2 STATEMENT OF WORK

B.3 PRICE/COST SCHEDULE

ITEM INFORMATION

B.4 DELIVERY SCHEDULE

SECTION C - CONTRACT CLAUSES

C.1 52.212-4 CONTRACT TERMS AND CONDITIONS—COMMERCIAL PRODUCTS

AND COMMERCIAL SERVICES (NOV 2023)

C.2 52.217-8 OPTION TO EXTEND SERVICES (NOV 1999)

C.3 VAAR 852.232-72 ELECTRONIC SUBMISSION OF PAYMENT REQUESTS (NOV

2018)

C.4 VAAR 852.242-71 ADMINISTRATIVE CONTRACTING OFFICER (OCT 2020)

C.5 52.252-2 CLAUSES INCORPORATED BY REFERENCE (FEB 1998)

C.6 52.217-9 OPTION TO EXTEND THE TERM OF THE CONTRACT (MAR 2000) ...42

C.7 52.212-5 CONTRACT TERMS AND CONDITIONS REQUIRED TO IMPLEMENT

STATUTES OR EXECUTIVE ORDERS—COMMERCIAL PRODUCTS AND

COMMERCIAL SERVICES (DEC 2023) (DEVIATION) (JAN 2024)

SECTION D - CONTRACT DOCUMENTS, EXHIBITS, OR ATTACHMENTS

NONE

SECTION E - SOLICITATION PROVISIONS

E.1 52.212-1 INSTRUCTIONS TO OFFERORS—COMMERCIAL PRODUCTS AND

COMMERCIAL SERVICES (SEP 2023)

E.2 52.204-24 REPRESENTATION REGARDING CERTAIN TELECOMMUNICATIONS

AND VIDEO SURVEILLANCE SERVICES OR EQUIPMENT (NOV 2021)

E.3 52.204-29 FEDERAL ACQUISITION SUPPLY CHAIN SECURITY ACT

ORDERS—REPRESENTATION AND DISCLOSURES (DEC 2023)

E.4 52.252-1 SOLICITATION PROVISIONS INCORPORATED BY REFERENCE (FEB

1998)

E.5 52.212-2 EVALUATION—COMMERCIAL PRODUCTS AND COMMERCIAL

SERVICES (NOV 2021)

E.6 52.212-3 OFFEROR REPRESENTATIONS AND CERTIFICATIONS—

COMMERCIAL PRODUCTS AND COMMERCIAL SERVICES (NOV 2023)

SECTION B - CONTINUATION OF SF 1449 BLOCKS

B.1 CONTRACT ADMINISTRATION DATA

1. Contract Administration: All contract administration matters will be handled by the following individuals:

a. CONTRACTOR: _______________________

b. GOVERNMENT: Astrid McKinney Contracting Officer 36C257 Ivan T Torres Contract Specialist

Department of Veterans Affairs NCO 17 North Texas Healthcare System Regional Procurement Office West (RPO-W) 5441 Babcock Rd. Ste.302 San Antonio TX 78240

2. CONTRACTOR REMITTANCE ADDRESS: All payments by the Government to the contractor will be made in accordance with:

[X] 52.232-33, Payment by Electronic Funds Transfer—System For Award Management, or

[X] 52.232-36, Payment by Third Party

3. INVOICES: Invoices shall be submitted in arrears:

a. Quarterly []

b. Semi-Annually []

c. Other [X] Monthly

4. GOVERNMENT INVOICE ADDRESS: All Invoices from the contractor shall be submitted electronically in accordance with VAAR Clause 852.232-72 Electronic Submission of Payment Requests.

This is accomplished through the Tungsten Network located at:

http://www.fsc.va.gov/einvoice.asp This is mandatory and the sole method for submitting invoices.

ACKNOWLEDGMENT OF AMENDMENTS: The offeror acknowledges receipt of amendments to the Solicitation numbered and dated as follows:

AMENDMENT NO DATE

B.2 STATEMENT OF WORK

Description of Services.

Scope of Work. The Contractor shall provide all personnel, transportation, and equipment. Services shall be performed by a licensed qualified diagnostic medical physicist. Contract is for Department of Veterans Affairs / South Texas Health Care System (STVHCS) AND OFF-SITE CLINICS for monthly, annual, and or emergent basis. These services will adhere to the requirements and expectations of The Joint Commission (TJC), VHA National Health Physics Program (NHPP), and the American College of Radiology (ACR), Mammography Quality Standards Act (MQSA), and Food and Drug Administration (FDA), and internal requirements of this facility where applicable. The Texas Department of State Health Services regulations contained in 25 TAC §289 are not in force at STVHCS but shall be followed as closely as practical.

All work shall be performed during business hours of 6:00 am to 4:30 PM Monday through Friday, except Federal Holidays. After hours and weekends shall be scheduled at least 30 days prior services (POC). To perform the following tasks:

Task 1: Annual review of STVHCS overall Imaging Quality Assurance program for diagnostic imaging equipment to include protocol reviews. [NHPP]

Task 2: Upon awarded of the vendor initiate STVHCS security/unescorted access requirements within 30 days of contract award. Credentialing process, to gain access to the desired service/department, the contractor must request STVHCS appropriate photo ID badge and authorization to proceed.

Task 3: Coordinate and schedule via email for annual review of STVHCS equipment copying COR, RSO, Biomedical Services and POC for each service (see Attachments B).

Task 4: Keep track and schedule Annual Equipment Performance Evaluations (EPE) as required.

Task 5: Establish or upgrade the Quality Assurance / Quality Control Program (QA/QC) to ensure compliance with Joint Commission, ACR.

Task 6: Annual, should not to exceed 12 months / shall not exceed 13 months, quality assurance testing survey and certification of all diagnostic x-ray and imaging equipment (to include MRI, and Nuclear Medicine). All equipment surveys should be scheduled with the COR and equipment’s service point of contact (POC) no later than 60 days prior to the survey but shall be scheduled not later than 30 days prior to survey. A scheduled shall be e-mailed to the RSO monthly. See Attachments A for list of existing equipment. This list may be modified (equipment added or removed) at any time. [TJC, NHPP]

Task 7: Recertification of imaging equipment prior to first patient use when required due to repairs or modification that may affect the radiation output or image quality. Within 24 hours of contact, the contractor will coordinate with the affected service (POC) and RSO to have the recertification scheduled.

Task 8: Written reports signed by the diagnostic medical physicist documenting the testing, including a summary of methods, instruments used, measurements and deficiencies identified, for all diagnostic x-ray and imaging equipment. The Contractor shall provide a copy of the physicist report to the COR, RSO, Biomedical Services and Chief of Service and POC for each service (see Attachments B) within (5) five working days of completion of the work. The report may be in electronic format. [TJC, NHPP]

Task 9: Deficiencies or non-conformances which represent unsafe conditions during inspection shall be verbally reported to the RSO, Biomedical Services, Chief of Services, and/or POC immediately prior to leaving facility. A log of deficiencies identified shall be reported to the COR and RSO on a monthly basis. The log at a minimum shall include the following: Service, EE#, deficiencies, date of deficiencies identified, date deficiencies corrected. Verbal reports must be provided after testing so that STVHCS will know that equipment can be immediately put into use.

Task 10: Dose rate surveys in unrestricted areas adjacent to the radiation areas are to be included during testing and in the final report.

Task 11: A patient exposure calculations will be performed for each unit inspected for common projections and procedures.

Task 12: Shielding design approvals for new construction and renovations.

Task 13: Shielding surveys for new construction, modifications, and replacement of equipment.

Task 14: Annual quality assurance testing of mammography review workstation and or attached printer. [MQSA]

Task 15: Support the STVHCS Radiation Safety Office by membership and attendance on the appropriate STVHCS committee meetings (i.e., Radiation Safety Committee, Image Quality Committee) on a quarterly or as needed basis. The STVHCS Radiation Safety Officer will request the diagnostic medical physicist to attend when expertise is required. [TJC]

Task 16: Provide as-needed medical radiation producing equipment training to STVHCS medical staff. The course will be a one-hour, hands-on training session designed to enhance the understanding and implementation of operational radiation protection principals to promote the reduction of occupational exposures to ionizing radiation in the clinical environment. The course content will to include: exposure (air kerma) outputs, high-level control options, occupational dose reduction techniques (positioning, shielding, and optimal equipment settings), and procedures for recording pertinent data.

Task 17: Provide consultation and final reports for dose estimates calculations for patient, staff, and fetal exposures; and sentinel event investigations.

Task 18: Twenty-four (24) hour emergency response time on unanticipated and/or emergent equipment needs.

Task 19: Participation in quarterly on-site review (4 meetings per year) of the technical Radimetrics QA program for all modalities. Assist STVHCS with establishing baseline Radimetrics QA thresholds. The review shall include a trend analysis of the Radimetrics QA data. Any trends that identify problems shall be discussed in the quality control meeting and included in the report along with recommendations corrective actions. The quality control meeting will include reviewing the CT protocol dose optimization. Reviewing CT protocols shall be completed at least annually with a signed copy furnished to the RSO.

The annual quality assurance testing will include all radiology and dental equipment at STVHCS – San Antonio, Kerrville, and off-site clinics. All quality assurance testing reports and mammography equipment performance evaluations reports shall be submitted to the STVHCS Radiation Safety Office for review and approval subsequent to the completion of all testing, calibration and surveys of the equipment, facilities and procedures. The reports shall identify all items of noncompliance and include general and specific recommendations for correcting any items of noncompliance. “All records (administrative and program specific) created during the period of the contract belong to VA South Texas Health Care System(STVHCS) and must be returned to STVHCS at the end of the contract or destroyed in accordance to the VHA Record Control Schedule (RCS)10-1.”

Period of Performance:

Base Year: April 15, 2024 to April 14, 2025 Option Year 1: April 15, 2025 to April 14, 2026

Option Year 2: April 15, 2026 to April 14, 2027 Option Year 3: April 15, 2027 to April 14, 2028 Option Year 4: April 15, 2028 to April 14, 2029

Acronyms:

AAPM American Association of Physicist in Medicine ACR American College of Radiology CBCT Cone Beam Computed Tomography CFR Code of Federal Regulations COR Contracting Officer Representative CT Computed Tomography FDA Food and Drug Administration FOV Field of View HVL Half Value Layer IEC International Electrotechnical Commission MQSA Mammography Quality Standards Act MRI Magnetic Resonance Imaging NCRP National Council for Radiation Protection NHPP National Health Physics Program PET Positron Emission Tomography POC Point of Contact QMP Qualified Medical Physicist QA Quality Assurance RSO Radiation Safety Officer SOW Statement of Work SPECT Single-Photon Emission Computed Tomography TJC The Joint Commission STVHCS South Texas Veterans Health Care System VHA Veterans Healthcare Administration

Quality Assurance Testing:

All Quality Assurance Tests shall meet or exceed current and possible future changes in NRC, ACR, MQSA, NHPP, NCRP, FDA and TJC requirements and recommendations. All Quality Assurance Tests shall meet or exceed the requirements in the following VHA directives and handbooks and future directives and handbooks:

VHA Directive 1105, Management of Radioactive Materials VHA Handbook 1105.02, Nuclear Medicine and Radiation Safety Administrative Service VHA Handbook 1105.03, Mammography Program Procedures and Standards VHA Handbook 1105.04, Fluoroscopy Safety VHA Handbook 1105.05, Magnetic Resonance (MR) Safety VHA Directive 1129, Radiation Protection for Machine Sources of Ionizing Radiation

Diagnostic X-ray Equipment (Radiography and Fluoroscopy):

The testing must include, but is not necessarily limited to, the following (as applicable):

Per VHA Handbook 1105.04, Fluoroscopy Safety:

Measurement of radiation output parameters, including beam intensity and beam quality;

Testing of all modes of operation used clinically, including automatic exposure rate controls of fluoroscopy systems;

Assessment of image quality;

Assessment of technique factors used clinically;

Measurement of appropriate indices of patient dose output chart must be generated for each survey in accordance 25 TAC. Dose rates at typical clinical technique factors, with comparison to national standards.

Per the American College of Radiology Technical Standard for Diagnostic Medical Physics Performance Monitoring of Radiologic and Fluoroscopic Equipment:

Integrity of unit assembly Collimation and radiation beam alignment Fluoroscopic system resolution

Automatic exposure control system performance Fluoroscopic automatic brightness control performance (high-dose-rate, pulsed modes, and field-of-view [FOV] variation) Image artifacts Fluoroscopic phantom image quality kVp accuracy and reproducibility Linearity of exposure versus mA or mAs Exposure reproducibility Timer accuracy Beam quality assessment (half-value layer) Fluoroscopic entrance exposure rates Image receptor entrance exposure Equipment radiation safety functions Patient dose monitoring system calibration Video and digital monitor performance within manufactures specifications compliance with standard of practice.

Digital image receptor performance

If the review of clinically-used technique factors or the comparison of measured dose indices with national standards indicates that an optimum balance has not been achieved between patient dose and image quality or that the dose indices exceed national standards, the technique factors, whether posted in a chart or programmed into the fluoroscope, must be modified as necessary. [VHA Handbook 1105.04]

Reports shall be generated indicating appropriate indices of patient dose, measured by a diagnostic medical physicist at clinically-used technique factors, to be posted near the controls of each fluoroscope. These indices include typical and maximal entrance skin dose or air kerma rate for each fluoroscopic mode of operation (e.g., pulse rate and magnification mode). For each image recording mode used clinically, these include the entrance skin dose or air kerma per image or the entrance skin dose or air kerma per second of imaging (e.g., cinefluorography in the cardiac catheterization laboratory) for a patient of typical thickness. [VHA Handbook 1105.04]

Computed Tomography:

The testing must include, but is not necessarily limited to, the following (as applicable):

Per the American College of Radiology Technical Standard for Diagnostic Medical Physics Performance Monitoring of Computed Tomography (CT) equipment:

Alignment light accuracy Image localization from scanned projection radiograph (localization image) Table incrementation accuracy Radiation beam width (collimation) Reconstructed image thickness Image quality o High-contrast (spatial) resolution o Low-contrast sensitivity and resolution o Image uniformity o Noise o Artifact evaluation

CT number accuracy Acquisition workstation display Dosimetry o Radiation output of CT scanner (CT dose index [CTDIvol] or equivalent) o Patient radiation dose estimate for representative examinations

Protocol review o The Diagnostic Medical Physicist can become a member of protocol review committee of the most commonly used protocols. These should include head and abdomen protocols for adult and pediatric patients as applicable to the facility’s practice. In addition, facility protocols for very high dose procedures (e.g., brain perfusion) should be reviewed.

o Elements reviewed should include documentation of kVp, mA, rotation time, detector configuration, pitch, reconstructed image thickness, and use of automatic exposure control (including ensuring documentation of reference settings used), and the indicated dose indices (CTDIvol) resulting from each examination.

Safety Evaluation o Visual inspection o Work load assessment o Scatter and stray radiation measurements (if work load and other related parameters have changed since acceptance testing) o Audible/visual signals o Posting requirements

Other tests as required by state or local regulations

Per the TJC Revised Requirements for Diagnostic Imaging Services (Prepublication Requirements; subject to change):

Image uniformity Slice thickness accuracy Slice position accuracy (when prescribed from a scout image) Alignment light accuracy Table travel accuracy Radiation beam width High-contrast resolution Low-contrast resolution Geometric or distance accuracy CT number accuracy and uniformity Artifact evaluation Dosimetry o The diagnostic medical physicist measures the radiation dose (in the form of volume computed tomography dose index [CTDIvol]) produced by each diagnostic CT imaging system for the following four CT protocols:

adult brain, adult abdomen, pediatric brain and pediatric abdomen. If one or more of these protocols is not used by the hospital, other commonly used CT protocols may be substituted.

o The diagnostic medical physicist verifies that the radiation dose (in the form of CTDIvol) displayed by the CT imaging system for each tested protocol is within 20 percent of the CTDIvol displayed on the CT console.

The dates, results, and verifications of these measurements are documented.

Image acquisition display monitors o Maximum luminance o Minimum luminance o Luminance uniformity o Resolution o Spatial accuracy

Dental:

The physics inspection shall conform to the Conference of Radiation Control Program Directors (CRCPD), Quality Control Recommendations for Diagnostic Radiography Volume 1 Dental Facilities July 2001. The performance of dental x-ray inspections shall be annually or every 2 years. This evaluation should include, but not be limited to, the following tests (as applicable):

Collimation Beam quality (half-value layer) Timer Accuracy and Reproducibility kVp Accuracy and Reproducibility mA or mAs Linearity Exposure Reproducibility Entrance skin exposure evaluation, with comparisons to published diagnostic reference levels and achievable doses (e.g. NCRP Report No. 172) Technique Chart Evaluation Image uniformity (artifact evaluation)

Dental Cone Beam Computed Tomography (CBCT) Acceptance and Performance Testing

a) Acceptance Testing. Acceptance testing and measurements of air kerma at the isocenter for each kVp station for a range of clinically used mAs settings will performed initially when the CBCT unit is installed, and following any move of the CBCT to another area inside or outside the initial clinical site. This testing is to ensure that the equipment performance is in agreement with the manufacturer’s technical specifications.

b) Performance Testing. Each CBCT unit shall undergo periodic quality control tests to ensure that the performance of the machine has not significantly deteriorated and is operating within the manufacturer’s technical specifications.

This performance testing is performed by a qualified expert annually, at intervals not to exceed 14 months, and after repairs to the CBCT unit that may affect the radiation output or image quality.

c) Some manufacturers provide a phantom and procedures to perform machine specific quality assurance (QA) tests.

In cases where the manufacturer provides a phantom and procedures to perform specific tests but the tests are not included in this SOW, then the manufacturer’s machine-specific QA tests shall be performed in addition to the QA tests in this SOW.

Acceptance and Annual physics testing for Dental CBCT

a) Radiation output Repeatability

Make four measurements of the air kerma at the isocenter at a clinically used setting. The measurements should be less than +/-5% of the average of the five measurements and the measurements should be less than +/- 5% of the previous year’s measurement.

b) Radiation Output Reproducibility

Measure the air kerma at the isocenter for each kVp station and a range of clinically used mAs setting. Compare the results to the baseline values established at the initial acceptance testing. The values should be +/-5% of the baseline.

c) kVp Accuracy

Measure the kVp at all clinically used settings. The measured kVp should be +/-5% of the selected kVp.

d) kVp Repeatability

Make five kVp measurements each for two clinically used kVp settings. All measured values should be +/-5% of the mean kVp.

e) kVp Reproducibility

Measure the kVp at all available kVp settings. The measured values should be +/-5% of the baseline.

f) Beam quality

Measure the half value layer (HVL) for aluminum. The minimum shall comply with Section F.4.d of the Suggested State Regulations for Control of Radiation, Conference of Radiation Control Program Directors.

g) Radiation field of view (FOV)

Measure the width of the radiation field at the isocenter. The width of the beam should be 3 mm or 30% of the total nominal collimated width.

h) Image Quality

Image the phantom provided by the manufacturer or another suitable phantom. Assess high contrast spatial resolution, uniformity of transaxial images, and image noise.

Imaging uniformity shall be assessed over the entire range of axial images.

i) Accuracy of Linear Measurements

Using images of an appropriate phantom, assess the accuracy of distance measurements.

j) Accuracy of Patient Dose Metric Indication

Assess the accuracy of the indicated dose metric (typically DAP).

k) Patient Dose Assessment

From a scan or scans using the facility’s standard techniques, record the dose metric (typically DAP) and compare to achievable levels and diagnostic reference levels (if available)

l) Review of the technical QA program The qualified expert shall review the technical QA program. The review shall include a trend analysis of the QA data.

The results of the technical QA program review shall be included in the written report. Any trends that identify problems shall be included in the report along with recommended corrective actions.

m) Display Monitors

Perform a visual analysis of the SMPTE test pattern.

i. Display the test pattern on the imaging console. Set the display window width/level to the manufacturer-specified values for the pattern. Do not set the window/level by eye; doing so invalidates the procedure.

ii. Examine the pattern to confirm that the gray level display in the imaging console is subjectively correct.

1. Review the line pair patterns in the center and at each of the corners.

2. Review the black-white transition.

3. Look for any evidence of “scalloping” (loss of bit depth) or geometric distortion.

iii. Use a photometer to measure the maximum and minimum monitor brightness (0% and 100% steps)

iv. Measure additional steps within the pattern to establish a response curve.

v. Measure the brightness near the center of the monitor and near all 4 corners (or all 4 sides, depending on the test pattern used).

n) Viewing Conditions

Assess the viewing conditions for the area in which the monitor used to evaluation the CBCT studies is located.

Mammography:

The qualified diagnostic medical physicist shall provide the facility with up to date documentation demonstrating they qualified diagnostic medical physicist is MQSA qualified. Inspections of mammography equipment must comply with the latest requirements posted on the ACR website for the manufacturer of the digital mammography unit being inspected. Inspection items may include:

Mammographic Unit Assembly Evaluation Mammographic Unit Assembly Evaluation Mammographic Unit Assembly Evaluation Collimation assessment Artifact evaluation kVp accuracy and reproducibility Beam quality assessment – HVL measurements Evaluation of system resolution Automatic Exposure Control (AEC) function performance Breast entrance exposure, AEC reproducibility and average glandular dose Radiation output rate Phantom image quality evaluation Signal–to–noise ratio and contrast – to noise ratio measurements Viewbox luminance and room illuminance Review workstation (RWS) tests

Mammography Display Monitors:

The physics inspection shall conform to the AAPM On-line Report No. 03, Assessment of Display Perform for Medical Imaging Systems. The performance of each display monitor shall be evaluated initially, acceptance testing, and at least annually thereafter. This evaluation should include, but not be limited to, the following tests (as applicable). Acceptance testing (Table 7 from AAPM On-line Report No. 03):

Geometric distortions Reflection Luminance response Luminance dependencies Resolution

Noise Veiling glare a low‐frequency degradation described by a point spread function (PSF).

Chromaticity Annual testing (Table 8c. from AAPM On-line Report No. 03)

Geometric distortions Reflection Luminance response Luminance dependencies Resolution Noise Veiling glare Chromaticity Mammography printers in accordance to MQSA requirements Grey artifacts Low contrast High contrast Evaluate ACR phantom from printer print out

For PET:

The physics inspection shall conform to the ACR PET Phantom Instructions for Evaluation of PET Image, ACR Nuclear Medicine Accreditation Program PET Module. The performance of each PET scanner shall be evaluated semiannually. For PET/CT units the CT must be inspected at least annually. This evaluation should include, but not be limited to, the following tests (as applicable):

Uniformity Spatial resolution SUV analysis Review quality control and radiation safety documents Phantom evaluation for PET scanner (semiannually) Evaluate acquisition work station (AWS) image quality

Nuclear Medicine:

The physics inspection shall conform to the ACR annual performance tests for nuclear medicine cameras. The performance of each nuclear medicine scanner shall be at least annually. The qualified diagnostic medical physics shall also perform the semiannually testing as outlined by the ACR. This evaluation should include, but not be limited to, the following tests (as applicable):

Intrinsic Uniformity: fail criteria: > 5.0% System Uniformity: fail criteria: > 5.0% Intrinsic or System Spatial Resolution: fail criteria > 3.5 mm bars Relative Sensitivity: fail criteria: COV > 2.5% Energy Resolution: fail criteria: >12% Count Rate Parameters: fail criteria Formatter/Video Display Overall System Performance for SPECT System Interlocks Dose Calibrators (Geometry (if applicable), Accuracy) Thyroid Uptake and Counting Systems Review quality control and radiation safety documents Phantom evaluation for Nuclear Medicine scanner (semiannually) Evaluate acquisition work station (AWS) image quality

MRI Equipment:

The testing must include, but is not necessarily limited to, the following (as applicable):

Per the American College of Radiology Technical Standard for Diagnostic Medical Physics Performance Monitoring of Magnetic Resonance Imaging (MRI) Equipment:

Magnetic field homogeneity Slice position accuracy

Slice thickness accuracy Radiofrequency (RF) calibration for all coils o Frequency and gain/attenuator verification (prescan values) o Image signal–to-noise ratio (SNR) for all coils o Intensity uniformity for all volume coils o Phase stability and image artifact assessment for all coils

Softcopy (monitor) fidelity Evaluation of quality control (QC) program

Per the TJC Revised Requirements for Diagnostic Imaging Services (Prepublication Requirements dated December 20, 2013; subject to change):

Image uniformity for all radiofrequency (RF) coils used clinically Signal-to-noise ratio (SNR) for all coils used clinically Slice thickness accuracy Slice position accuracy Alignment light accuracy High-contrast resolution Low-contrast resolution (or contrast-to-noise ratio) Geometric or distance accuracy

Magnetic field homogeneity Artifact evaluation Image acquisition display monitors o Maximum luminance o Minimum luminance o Luminance uniformity o Resolution o Spatial accuracy

Structural Shielding:

For any room in which a fluoroscopic imaging system is installed, or in which a mobile fluoroscopic imaging system is frequently used, the doses to persons in adjacent areas, including any areas above and below, must be evaluated by a diagnostic medical physicist or medical health physicist. Structural shielding must be installed as necessary to maintain doses to persons in these areas ALARA and within regulatory limits. [VHA Handbook 1105.04]

For the structural shielding of rooms containing x-ray imaging devices, the shielding design goal must be 5 milligray (mGy) in a year to any person in a controlled area. For uncontrolled areas, the shielding design goal needs to be 1 mGy in a year to any person, and 0.02 mGy in any hour. [VHA Handbook 1105.04]

The design of shielding for and acceptance testing surveys of imaging rooms must conform to National Council on Radiation Protection and Measurements (NCRP) Report No. 147, Structural Shielding Design for Medical X-ray Imaging Facilities. The shielding design calculations, as-built shielding plans, and the report on the acceptance testing of the structural shielding must be kept for the duration of use of the room for x-ray imaging. [VHA Handbook 1105.04]

Qualifications. Prior to commencing work, all contractor employees shall meet certain criteria to perform work under this contract as a Diagnostic Medical Physicist. Qualification documents must be submitted as part of the bid to the Contracting Officer and be approved by the RSO or his/her designee. All qualifications are subject to review by the STVHCS Chief of Radiation Safety Service.

Diagnostic Medical Physicist:

The Diagnostic Medical Physicist who performs the work at STVHCS shall meet the following education, certification, and qualification standards:

Hold a Masters Degree or higher in Medical Physics, Health Physics or a related field.

Hold current Board Certification by the American Board of Radiology or American Board of Medical Physics.

Licensed by the State of Texas as a Professional Medical Physicist.

Licensed with up to date documentation of MQSA qualifications.

Meet all NRC, ACR, MQSA, FDA and TJC requirements for a qualified diagnostic medical physicist.

The qualified diagnostic medical physicist inspecting mammography equipment must meet the qualifications outline in the Mammography Quality Standards Act (MQSA).

A physicist assistant personally must be accompanied and supervised by a fully licensed qualified diagnostic medical physicist.

A temporary license medical physicist must be supervised as defined by: Temporary Medical Physicist Supervisor Agreement Plan for Texas.

The Diagnostic Medical Physicist shall have current knowledge, understanding, and recent experience in the following:

Texas Department of State Health Services, Radiation Control Regulations

Current NRC regulations

Current FDA regulations (including MQSA)

Current recommendations of the ACR and TJC on diagnostic x-ray and imaging equipment

Current recommendations of the NCRP and AAMP on medical imaging facility design and shielding

Current techniques for the calibration and testing of diagnostic x-ray equipment

Period of Performance will be from April 15, 2024 thru April 14, 2025 and four (4) Option Years. This contract will include one base with four option periods (each option period is equal to one year).

Period of Performance:

Base Year: April 15, 2024 to April 14, 2025

Option Year 1: April 15, 2025 to April 14, 2026 Option Year 2: April 15, 2026 to April 14, 2027 Option Year 3: April 15, 2027 to April 14, 2028

Option Year 4: April 15, 2028 to April 14, 2029

Contractor Personnel Security Requirements - Information Systems Access

Upon contract award, all personnel with access to the facility shall be subject to the appropriate type of background investigation or screening per VA/VHA policy as delineated below, and must receive a favorable adjudication from the local VA facility or VA Security and Investigations Center (SIC) depending on the type of investigation/screening required. This requirement is also applicable to all subcontract personnel.

Contract personnel who previously received a favorable adjudication as a result of a Government background investigation or screening may be exempt from this contract requirement provided that they can provide documentation to support the previous adjudication. Proof of previous adjudication must be submitted by the Contractor to VA Contracting Officer. Proof of previous adjudication is subject to verification. Some positions maybe subject to periodic re-investigation/screening.

Position Risk/Sensitivity. For all positions required under this contract, the position risk/sensitivity has been designated as:

Low Risk/Non-Sensitive.

Prior to completing the required forms, contract personnel should review the attachments entitled Common Errors on NACI Security Questionnaires, Example_SF85, Example_OF306, and General Questions and Answers about OPM background Investigations (see item 3.2 of this contract for these attachments) in order to ensure the forms are properly completed. Please note that incomplete forms will be rejected and could result in a delay of work under the contract.

Once the items requested are received, VA will pre-screen these items for completeness, and forward them to the appropriate party(s) in order to initiate the required background investigation(s) or screening(s) within fourteen (14) calendar days of appointment. Only after the VA Contracting Officer notifies the Contractor that the background investigation(s) or screening(s) was initiated shall the Contractor be authorized to provide services under the contract.

The Contractor, when notified of an unfavorable determination by the Government, shall withdraw the contract person from consideration of working under the contract.

Failure to comply with these Contractor personnel security requirements may result in termination of the contract for default.

CONTRACTOR PERSONNEL SECURITY REQUIREMENTS

Position Sensitivity – The position sensitivity has been designated as Low Risk/Non-sensitive.

a. Background Investigation – Upon contract award, all personnel with access to the facility shall be subject to the appropriate type of background investigation or screening per VA/VHA policy, and must receive a favorable adjudication from the local VA facility or VA Security and Investigations Center (SIC) depending on the type of investigation/screening required.

b. Contractor Responsibilities

(1) The Contractor shall submit or ensure that their employees submit the required information to the Contracting Officer and Contracting Officer’s Representative (COR). The Contractor shall submit the required forms to the VA Security and Investigations Center within 5 days of receipt of the e-mail with instructions to do so. The Contractor shall not allow Contractor personnel who require a background investigation to start performing until the Contractor has received written confirmation from the Contracting Officer that the SIC has initiated a background investigation.

(2) The Contractor, when notified of and unfavorable determination by the Government, shall withdraw the employee from consideration from working under the contract.

(3) Unless written authorization is issued by the Contracting Officer, contractor employees will not use any form of removable storage media when providing services under the terms of this contract. Removable storage media includes, but is not limited to, USB thumb drives, MP3 Players, and external hard drives. Should the Contractor determine that the use of removable storage devices is required they must submit a written request with full justification to the Contracting Officer.

Failure to comply of with the contractor personnel security requirements may result in termination of the contract for default.

Information Security

The diagnostic medical physicist working with the contractor may have access to sensitive patient information displayed on the control panel of X-ray equipment. However, contractor owned IT devices (such as laptop computer) shall not interface with any VA internet trusted (i.e., non-public) network. Therefore, the certification and accreditation (C&A) requirements do not apply, and a Security Accreditation Package is not required. Contractor shall not print or copy any sensitive patient information.

GENERAL

Contractors, contractor personnel, subcontractors, and subcontractor personnel shall be subject to the same Federal laws, regulations, standards, and VA Directives and Handbooks as VA and VA personnel regarding information and information system security.

ACCESS TO VA INFORMATION AND VA INFORMATION SYSTEMS

a. A contractor/subcontractor shall request logical (technical) or physical access to VA information and VA information systems for their employees, subcontractors, and affiliates only to the extent necessary to perform the services specified in the contract, agreement, or task order.

b. All contractors, subcontractors, and third-party servicers and associates working with VA information are subject to the same investigative requirements as those of VA appointees or employees who have access to the same types of information. The level and process of background security investigations for contractors must be in accordance with VA Directive and Handbook 0710, Personnel Suitability and Security Program. The Office for Operations, Security, and Preparedness is responsible for these policies and procedures.

c. Contract personnel who require access to national security programs must have a valid security clearance. National Industrial Security Program (NISP) was established by Executive Order 12829 to ensure that cleared U.S. defense industry contract personnel safeguard the classified information in their possession while performing work on contracts, programs, bids, or research and development efforts. The Department of Veterans Affairs does not have a Memorandum of Agreement with Defense Security Service (DSS). Verification of a Security Clearance must be processed through the Special Security Officer located in the Planning and National Security Service within the Office of Operations, Security, and Preparedness.

d. Custom software development and outsourced operations must be located in the U.S. to the maximum extent practical. If such services are proposed to be performed abroad and are not disallowed by other VA policy or mandates, the contractor/subcontractor must state where all non-U.S. services are provided and detail a security plan, deemed to be acceptable by VA, specifically to address mitigation of the resulting problems of communication, control, data protection, and so forth. Location within the U.S. may be an evaluation factor

e. The contractor or subcontractor must notify the Contracting Officer immediately when an employee working on a VA system or with access to VA information is reassigned or leaves the contractor or subcontractor’s employ. The Contracting Officer must also be notified immediately by the contractor or subcontractor prior to an unfriendly termination.

VA INFORMATION CUSTODIAL LANGUAGE

a. Information made available to the contractor or subcontractor by VA for the performance or administration of this contract or information developed by the contractor/subcontractor in performance or administration of the contract shall be used only for those purposes and shall not be used in any other way without the prior written agreement of the VA. This clause expressly limits the contractor/subcontractor's rights to use data as described in Rights in Data - General, FAR 52.227-14(d) (1).

b. VA information should not be co-mingled, if possible, with any other data on the contractors/subcontractor’s information systems or media storage systems in order to ensure VA requirements related to data protection and media sanitization can be met. If co-mingling must be allowed to meet the requirements of the business need, the contractor must ensure that VA’s information is returned to the VA or destroyed in accordance with VA’s sanitization requirements.

VA reserves the right to conduct on site inspections of contractor and subcontractor IT resources to ensure data security controls, separation of data and job duties, and destruction/media sanitization procedures are in compliance with VA directive requirements.

c. Prior to termination or completion of this contract, contractor/subcontractor must not destroy information received from VA, or gathered/created by the contractor in the course of performing this contract without prior written approval by the VA. Any data destruction done on behalf of VA by a contractor/subcontractor must be done in accordance with National Archives and Records Administration (NARA) requirements as outlined in VA Directive 6300, Records and Information Management and its Handbook 6300.1 Records Management Procedures, applicable VA Records Control Schedules, and VA Handbook 6500.1, Electronic Media Sanitization. Self-certification by the contractor that the data destruction requirements above have been met must be sent to the VA Contracting Officer within 30 days of termination of the contract.

d. The contractor/subcontractor must receive, gather, store, back up, maintain, use, disclose and dispose of VA information only in compliance with the terms of the contract and applicable Federal and VA information confidentiality and security laws, regulations and policies. If Federal or VA information confidentiality and security laws, regulations and policies become applicable to the VA information or information systems after execution of the contract, or if NIST issues or updates applicable FIPS or Special Publications (SP) after execution of this contract, the parties agree to negotiate in good faith to implement the information confidentiality and security laws, regulations and policies in this contract.

e. The contractor/subcontractor shall not make copies of VA information except as authorized and necessary to perform the terms of the agreement or to preserve electronic information stored on contractor/subcontractor electronic storage media for restoration in case any electronic equipment or data used by the contractor/subcontractor needs to be restored to an operating state. If copies are made for restoration purposes, after the restoration is complete, the copies must be appropriately destroyed.

f. If VA determines that the contractor has violated any of the information confidentiality, privacy, and security provisions of the contract, it shall be sufficient grounds for VA to withhold payment to the contractor or third party or terminate the contract for default or terminate for cause under Federal Acquisition Regulation (FAR) part 12.

g. If a VHA contract is terminated for cause, the associated BAA must also be terminated and appropriate actions taken in accordance with VHA Handbook 1600.01, Business Associate Agreements. Absent an agreement to use or disclose protected health information, there is no business associate relationship.

h. The contractor/subcontractor must store, transport, or transmit VA sensitive information in an encrypted form, using VA-approved encryption tools that are, at a minimum, FIPS 140-2 validated.

i. The contractor/subcontractor’s firewall and Web services security controls, if applicable, shall meet or exceed VA’s minimum requirements. VA Configuration Guidelines are available upon request.

j. Except for uses and disclosures of VA information authorized by this contract for performance of the contract, the contractor/subcontractor may use and disclose VA information only in two other situations: (i) in response to a qualifying order of a court of competent jurisdiction, or (ii) with VA’s prior written approval. The contractor/subcontractor must refer all requests for, demands for production of, or inquiries about, VA information and information systems to the VA contracting officer for response.

k. Notwithstanding the provision above, the contractor/subcontractor shall not release VA records protected by Title 38 U.S.C. 5705, confidentiality of medical quality assurance records and/or Title 38 U.S.C. 7332, confidentiality of certain health records pertaining to drug addiction, sickle cell anemia, alcoholism or alcohol abuse, or infection with human immunodeficiency virus. If the contractor/subcontractor is in receipt of a court order or other requests for the above mentioned information, that contractor/subcontractor shall immediately refer such court orders or other requests to the VA contracting officer for response.

l. For service that involves the storage, generating, transmitting, or exchanging of VA sensitive information but does not require C&A or an MOU-ISA for system interconnection, the contractor/subcontractor must complete a Contractor Security Control Assessment (CSCA) on a yearly basis and provide it to the COTR.

LIQUIDATED DAMAGES FOR DATA BREACH

a. Consistent with the requirements of 38 U.S.C. §5725, a contract may require access to sensitive personal information.

If so, the contractor is liable to VA for liquidated damages in the event of a data breach or privacy incident involving any SPI the contractor/subcontractor processes or maintains under this contract.

b. The contractor/subcontractor shall provide notice to VA of a “security incident” as set forth in the Security Incident Investigation section above. Upon such notification, VA must secure from a non-Department entity or the VA Office of Inspector General an independent risk analysis of the data breach to determine the level of risk associated with the data breach for the potential misuse of any sensitive personal information involved in the data breach. The term 'data breach' means the loss, theft, or other unauthorized access, or any access other than that incidental to the scope of employment, to data containing sensitive personal information, in electronic or printed form, that results in the potential compromise of the confidentiality or integrity of the data. Contractor shall fully cooperate with the entity performing the risk analysis.

Failure to cooperate may be deemed a material breach and grounds for contract termination.

c. Each risk analysis shall address all relevant information concerning the data breach, including the following:

(1) Nature of the event (loss, theft, unauthorized access);

(2) Description of the event, including:

(a) date of occurrence;

(b) data elements involved, including any PII, such as full name, social security number, date of birth, home address, account number, disability code;

(3) Number of individuals affected or potentially affected;

(4) Names of individuals or groups affected or potentially affected;

(5) Ease of logical data…