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FBO DAILY - FEDBIZOPPS ISSUE OF SEPTEMBER 14, 2016 FBO #5409
DOCUMENT

Q -- Pathology Tests Intent to Sole Source Notice - Attachment

Notice Date

9/12/2016
 

Notice Type

Attachment
 

NAICS

621511 — Medical Laboratories
 

Contracting Office

Department of Veterans Affairs;Network Contracting Office 20;5115 NE 82nd Ave, Suite 102;Vancouver WA 98662
 

ZIP Code

98662
 

Solicitation Number

VA26016N0960
 

Archive Date

9/17/2016
 

Point of Contact

Laura Patterson
 

Small Business Set-Aside

N/A
 

Description

Intent to Sole Source: University of Washington Special Notice Number: VA26016AP6299 THIS IS A NOTICE OF INTENT TO AWARD A SOLE SOURCE CONTRACT AND IS NOT A REQUEST FOR COMPETITIVE QUOTES. Department of Veterans Affairs, Network Contracting Office (NCO) 20, anticipates making a sole source award under statutory authority 41 U.S.C. 253(c) and FAR 13.106-1(b) (1) (i), only one responsible source, with: University of Washington, UW Pathology - Reference Lab, 1959 NE Pacific Street, Seattle, WA 98195. The objective of this sole source award is to procure all the following pathology tests as listed in Tables A-D below. Turnaround time will not exceed 72 hours or 3 working days. The NAICS code for this requirement is 621511. This notice of intent is not a request for competitive quotes; however, interested persons may identify their interest and capability to respond to this requirement. Information received by 11:00 AM Pacific Time on September 16, 2016 may be considered by the Government. Responses shall be submitted to Laura Patterson at laura.patterson3@va.gov. The email subject line shall state, "Special Notice Number VA26016AP6299." A determination by the Government not to compete with this proposed contract based upon responses to this notice is solely within the discretion of the Government. Information received will normally be considered solely for the purpose of determining whether to conduct a competitive procurement. NO TELEPHONE REQUESTS WILL BE HONORED Table A: General Anatomic Pathology Reference Lab Test List CPT Description 84311-TCSPECTROPHOTOMETRY 87491-TCCHLAMYDIA TRACHOMATIS, AMPLIFIED PROBE TECHNIQUE 87591-TCNEISSERIA GONORRHOEAE, AMPLIFIED PROBE TECHNIQUE 87621-TCIADNA PAPLMVIRUS HUMAN AMP PRB 88104-TCCYTP FLU WASHGS/BRUSHINGS XCPT CIV SMRS INTERPJ 88104-26CYTP FLU WASHGS/BRUSHINGS XCPT CIV SMRS INTERPJ 88108-TCCYTP CONCENTRATION SMRS&INTERPJ 88108-26CYTP CONCENTRATION SMRS&INTERPJ 88112-TCCYTP SLCTV CELL ENHANCEMENT INTERPJ XCPT CIV 88112-26CYTP SLCTV CELL ENHANCEMENT INTERPJ XCPT CIV 88120-TCCYTP INSITU HYBRID URINE SPEC 3-5 PROBES EA MNL 88120-26CYTP INSITU HYBRID URINE SPEC 3-5 PROBES EA MNL 88125-TCFORENSIC CYTOPATHOLOGY 88125-26FORENSIC CYTOPATHOLOGY 88141-TCCYTOPATH CIV INTERPRET 88142-TCCYTP CIV FLU AUTO THIN MNL PHYS 88143-TCCYTP CIV FLU AUTO THIN MNL SCR&RESCR PHYS 88150-TCCYTOPATH CIV MANUAL 88153-TCCYTOPATH CIV REDO 88160-TCCYTOPATH SMEAR OTHER SOURCE 88160-26CYTOPATH SMEAR OTHER SOURCE 88162-TCCYTOPATH SMEAR OTHER SOURCE 88162-26CYTOPATH SMEAR OTHER SOURCE 88164-TCCYTOPATH TBS CIV MANUAL 88165-TCCYTOPATH TBS CIV REDO 88172-TCCYTP FINE NDL ASPIRATE IMMT CYTOHIST STD DX 1ST 88172-26CYTP FINE NDL ASPIRATE IMMT CYTOHIST STD DX 1ST 88173-TCCYTP FINE NDL ASPIRATE I&R 88173-26CYTP FINE NDL ASPIRATE I&R 88177-TCCYTP CIV AUTO THIN LYR PREPJ ADEQUACY EA EVAL 88177-26CYTP CIV AUTO THIN LYR PREPJ ADEQUACY EA EVAL 88182-TCFLO CYTOMETRY CELL CYCLE/DNA ALYS 88182-26FLO CYTOMETRY CELL CYCLE/DNA ALYS 88184-TCFLO CYTOMETRY CELL SURF MARKER TECHL ONLY 1ST 88185-TCFLOWCYTOMETRY/TC ADD-ON 88230-TCTISS CUL NON-NEO DISORDERS LYMPHOCYTE 88237-TCTISS CUL NEO DISORDERS B1 MARROW BLD CELLS 88239-TCTISS CUL NEO DISORDERS SOLID TUM 88262-TCCHRMSM CNT 15-20 CLL 2KARYOTYP BANDING 88264-TCCHRMSM ANALYZE 20-25 CELLS 88271-TCMOLEC CYTOGENETICS DNA PRB EA 88273-TCMOLEC CYTG CHRMOML ISH 10-30 CLL 88275-TCMOLEC CYTG INTERPHASE ISH ANALYZE 100-300 CLL 88291-26CHROMOSOME STUDY ADDITIONAL 88302-TCLVL II-SURG PATH GROSS&MCRSCP XM 88302-26LVL II-SURG PATH GROSS&MCRSCP XM 88304-TCLEVEL III-SURG PATH GROSS&MICROSCOPIC XM 88304-26LEVEL III-SURG PATH GROSS&MICROSCOPIC XM 88305-TCLVL IV-SURG PATH GROSS&MCRSCP XM 88305-26LVL IV-SURG PATH GROSS&MCRSCP XM 88307-TCLVL V-SURG PATH GROSS&MCRSCP XM 88307-26LVL V-SURG PATH GROSS&MCRSCP XM 88309-TCLVL VI-SURG PATH GROSS&MCRSCP XM 88309-26LVL VI-SURG PATH GROSS&MCRSCP XM 88311-TCDECALCIFICATION PX 88311-26DECALCIFICATION PX 88312-TCSPECIAL STAINS GROUP 1 MICROORGANISMS I&R EACH 88312-26SPECIAL STAINS GROUP 1 MICROORGANISMS I&R EACH 88313-TCSPECIAL STAINS GROUP II ALL OTHER I&R EACH 88313-26SPECIAL STAINS GROUP II ALL OTHER I&R EACH 88314-TCSPECIAL STAINS HISTOCHEMICAL W/FROZEN SECTION 88314-26SPECIAL STAINS HISTOCHEMICAL W/FROZEN SECTION 88319-TCDETERMINATIVE HCHEM/CCHEM ID NZM EA 88319-26DETERMINATIVE HCHEM/CCHEM ID NZM EA 88321-26CONSLTJ&REPRT SLIDES PREPARED ELSEWHERE 88323-TCCONSLTJ&REPRT MATRL REQ PREPJ SLIDES 88323-26CONSLTJ&REPRT MATRL REQ PREPJ SLIDES 88325-TCCOMPREHENSIVE REVIEW OF DATA 88329-TCPATH CONSULT INTROP 88331-TCPATH CONSLTJ SURG 1ST BLK FROZEN SCTJ 1 SPEC 88331-26PATH CONSLTJ SURG 1ST BLK FROZEN SCTJ 1 SPEC 88332-TCPATH CONSLTJ SURG EA BLK FROZEN SCTJ 88332-26PATH CONSLTJ SURG EA BLK FROZEN SCTJ 88333-TCPATH CONSLTJ SURG CYTOLOGIC XM 1ST SIT 88333-26PATH CONSLTJ SURG CYTOLOGIC XM 1ST SIT 88334-TCPATH CONSLTJ SURG CYTOL XM EA ADDL 88334-26PATH CONSLTJ SURG CYTOL XM EA ADDL 88341-TCIMHISTOCHEM/CYTCHM INIT ANTIBODY STAIN PROCEDURE 88341-26IMHISTOCHEM/CYTCHM INIT ANTIBODY STAIN PROCEDURE 88342-TCIMCYTCHM TISS IMMUNOPROXIDASE EA ANTB 88342-26IMCYTCHM TISS IMMUNOPROXIDASE EA ANTB 88346-TCIMFLUOR STD EA ANTB DIR METH 88346-26IMFLUOR STD EA ANTB DIR METH 88348-TCELECTRON MIC DX 88348-26ELECTRON MIC DX 88350-TCIMMUNOFLUORESCENCE PER SPEC ADD SINGL ANTB STAIN 88350-26IMMUNOFLUORESCENCE PER SPEC ADD SINGL ANTB STAIN 88360-TCTUMOR IMMUNOHISTOCHEM/MANUAL 88360-26TUMOR IMMUNOHISTOCHEM/MANUAL 88362-TCNRV TEASING PREPJS 88362-26NRV TEASING PREPJS 88363-TCEXAM & SELECT ARCHIVE TISSUE MOLECULAR ANALYSIS 88365-TCSITU HYBRIDIZATION EA PRB 88365-26SITU HYBRIDIZATION EA PRB 88368-TCM/PHMTRC ALYS ISH EA PRB MNL 88368-26M/PHMTRC ALYS ISH EA PRB MNL 88387-TCTISS EXAM MOLECULAR STUDY 88387-26TISS EXAM MOLECULAR STUDY 88388-TCTISS EX MOLECUL STUDY ADD-ON 88388-26TISS EX MOLECUL STUDY ADD-ON TC = Technical Component 26 = Professional Component Table B: Northwest Clinical Genomics Lab Test List CPT(s)Test Description 81415Amyotrophic Lateral Sclerosis (ALS) Exome Panel 81415Cardiac Arrhythmia Exome Panel 81415Cardiomyopathy Exome Panel 81415Comprehensive Cardiac Arrhythmia / Cardiomyopathy Exome Panel 81415Comprehensive Dementia, Parkinson's, ALS Exome Panel 81415Dementia Exome Panel 81415Exome Panel On Demand 81415Exome Sequence Analysis 81415Exome Sequence Comparator 81417Exome Re-evaluation of Previously Obtained Sequence 81415Genome Sequence Analysis 81426Genome Sequence Analysis Comparator 81426Genome Re-evaluation of Previously Obtained Sequence 81415Parkinson's Disease Exome Panel 81417REFLEX to Exome Sequencing 81403 or 81479Testing for Known Pathogenic Variant Table C: Collagen Diagnostic Laboratory Test List Test NameGene(s) CPT(s) COL1A1 and COL1A2 gDNA SequencingCOL1A1, COL1A2 81408 x 2 Dominant OI PanelCOL1A1, COL1A2, IFITM581408 x 2, 81479 x 1 Dominant OI Panel plus PLS3COL1A1, COL1A2, IFITM5, PLS381408 x 2, 81479 x 2 Recessive OI Panel plus ALPLCRTAP, FKBP10, LEPRE1, PPIB, PLOD2, SERPINH1, SERPINF1, SP7, SMP1, TMEM38B, WNT1, CREB3L1, ALPL81479 Autosomal Dominant and Recessive OI PanelCOL1A1, COL1A2, IFITM5, PLS3, CRTAP, FKBP10, LEPRE1, PPIB, PLOD2, SERPINH1, SERPINF1, SP7, SMP1, TMEM38B, WNT1, CREB3L1, ALPL81479 Classical EDS PanelCOL5A1, COL5A281479 Core EDS PanelCOL5A1, COL5A2, COL3A181479 Core Familial Aneurysm Panel ACTA2, COL3A1, TGFBR1, TGFBR2, TGFB2, SMAD3, FBN1, MYH11, MYLK, PRKG1, SLC2A10, TGFB3, NOTCH1, SKI, FBN2, FOXE381410 Marfan Syndrome and Loeys-Dietz Panel FBN1, TGFBR1, TGFBR2, TGFB2, TGFB3, SMAD381479 Extended Marfan-Related Disorders PanelFBN1, TGFBR1, TGFBR2, TGFB2, TGFB3, SMAD3, SKI, FBN281479 Alport PanelCOL4A3, COL4A4, COL4A581408 x 2, 81407 x 1 Hereditary angiopathy/Incracranial hemorrhageCOL4A1, COL4A281408, 81479 FBN1 genomic sequencingFBN181408 COL3A1 genomic sequencingCOL3A181479 TGFBR1 and TGFBR2 genomic sequencingTGFBR1, TGFBR281405 x 2 Bruck SyndromeFKBP10, PLOD281479 x 2 Caffey DiseaseTargeted COL1A181403 HypophosphatasiaALPL81479 X-Linked OsteoporosisPLS381479 EDS type VIExon 6 COL1A1 and COL1A281479 x 2 FKBP14-Related EDSFKBP1481479 IFITM5 genomic sequencingIFITM581479 PLOD1 genomic sequencingPLOD181479 ACTA2 genomic sequencingACTA281405 SMAD3 genomic sequencingSMAD381479 SLC2A10 genomic sequencingSLC2A1081479 TGFB2 genomic sequencingTGFB281479 TGFB3 genomic sequencingTGFB381479 MYH11 genomic sequencingMYH1181408 MYLK genomic sequencingMYLK81479 PRKG1 genomic sequencingPRKG181479 BMP1 genomic sequencingBMP181479 FKBP10 genomic sequencingFKBP10 81479 CREB3L1 genomic sequencingCREB3L181479 CRTAP genomic sequencingCRTAP 81479 P3H1 genomic sequencingP3H181479 PLOD2 genomic sequencingPLOD281479 PPIB genomic sequencingPPIB81479 SERPINF1 genomic sequencingSERPINF181479 SERPINH1 genomic sequencingSERPINH181479 SP7/OSX genomic sequencingSP7/OSX81479 TMEM38B genomic sequencingTMEM38B81479 WNT1 genomic sequencingWNT181479 X-Linked Alport SyndromeCOL4A1 81408 Prenatal TestingAll genes81479 Testing for Familial Pathogenic VariantKnown Mutation Testing of COL1A1, COL1A2, TGFBR1, TGFBR2, FBN1 and ACTA281403 Testing for Familial Pathogenic VariantKnown Mutation Testing of all other genes (COL2A1, SMAD3, P3H1, etc.)81479 Deletion/Duplication AnalysisAll genes81228 Deletion/Duplication Analysis (additional gene) G0452 Maternal Cell Contamination Studies 81465 COL1A1 and COL1A2 gDNA SequencingCOL1A1, COL1A2 81408 x 2 Dominant OI PanelCOL1A1, COL1A2, IFITM581408 x 2, 81479 x 1 Dominant OI Panel plus PLS3COL1A1, COL1A2, IFITM5, PLS381408 x 2, 81479 x 2 Recessive OI Panel plus ALPLCRTAP, FKBP10, LEPRE1, PPIB, PLOD2, SERPINH1, SERPINF1, SP7, SMP1, TMEM38B, WNT1, CREB3L1, ALPL81479 Classic EDS PanelCOL5A1, COL5A281479 Alport PanelCOL4A3, COL4A4, COL4A581408 x 2, 81407 x 1 FBN1 genomic sequencingFBN181408 COL3A1 genomic sequencingCOL3A181479 Table D: Clinical Cytogenomics/Array Lab Test List Test NameGenesCPT(s) Constitutional Cytogenomic Microarray AnalysisWhole Genome81229, G0452 Neoplasia Cytogenomic Microarray AnalysisWhole Genome81229, G0452 Y Chromosome Microdeletion AnalysisAMELY, CDY1, DA, DBY, HSFY1, RBMY1, SRY, USP9Y81403
 

Web Link

FBO.gov Permalink
(https://www.fbo.gov/notices/f5a327bb1f6255efe87f78f2ee70bff1)
 

Document(s)

Attachment
 

File Name: VA260-16-N-0960 VA260-16-N-0960_1.docx (https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=2999894&FileName=VA260-16-N-0960-000.docx)

Link: https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=2999894&FileName=VA260-16-N-0960-000.docx

 

Note: If links are broken, refer to Point of Contact above or contact the FBO Help Desk at 877-472-3779.
 

Record

SN04266266-W 20160914/160912234511-f5a327bb1f6255efe87f78f2ee70bff1 (fbodaily.com)
 

Source

FedBizOpps Link to This Notice
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