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FBO DAILY - FEDBIZOPPS ISSUE OF JULY 30, 2016 FBO #5363
SPECIAL NOTICE

65 -- Cost Per Test for BioPlex 2200 - Notice of Intent

Notice Date
7/28/2016
 
Notice Type
Special Notice
 
NAICS
511210 — Software Publishers
 
Contracting Office
Department of the Navy, Bureau of Medicine and Surgery, Naval Medical Logistics Command, 693 Neiman Street, FT Detrick, Maryland, 21702-9203, United States
 
ZIP Code
21702-9203
 
Solicitation Number
N62645-12-D-5053
 
Archive Date
9/30/2016
 
Point of Contact
Yun P. Hong, Phone: 3016194162
 
E-Mail Address
yun.p.hong.civ@mail.mil
(yun.p.hong.civ@mail.mil)
 
Small Business Set-Aside
N/A
 
Description
Cost Per Test for Bio-Plex 2200. The Naval Medical Logistics Command (NMLC) intends to negotiate on a sole source basis (IAW FAR Part 13.501(a)) on behalf of Naval Medical Center San Diego (NMCSD). The current contract, N62645-12-D-5053, is awarded to Government Scientific Source, 12351 Sunrise Valley Drive, Reston, VA 20191. NMCSD has a need to increase the current requirement for a cost per reportable test contract for a multi-technology laboratory analyzer (BioPlex 2200), reagents, calibrators and control items. The system allows for full automation from the time of adding the specimen to the analysis of results and transfer for those results to the Laboratory Information System (LIS). The system is capable of detecting serological immune markers directly from human plasma. The system uses flow cytometry based technology and fluorescent microbeads to detect multiple targets simultaneously from patient plasma. The system has random-access allowing different tests to be performed on samples without requiring users to organize, group, or batch specimens to perform testing. The system is capable of multiplex analysis through the performance of different tests simultaneously on each individual specimen. Automated steps in the specimen processing shall include; specimen processing, incubation, wash steps, analysis, and data distribution. The system is capable of processing at least 50 patient specimens per hour, with multiple tests capable of being performed simultaneously on each specimen. The system is capable of process samples randomly directly from sample tubes. Sample analysis includes detection of at least 50 beads/assay sample size markers. The system is capable of testing for: Measles IgG, Mumps IgG, Rubella IgG, Varicella IgG, Toxoplasma IgM/IgG, Cytomegalovirus IgM/IgG, Herpes Simplex Virus 1 and 2 IgG, Epstein-Barr Virus IgM/IgG markers (EAD, EBNA, VCA), and Treponema pallidum (Syphilis) IgG. The system is able to screen for autoimmune anti-nuclear antibodies (ANA) as a panel. The system is capable of differentiating between the following markers without requiring additional testing: dsDNA, Chromatin DNP, ribosomal P, ss-A, ss-B, Sm, Sm/RNP, Scl-70, Jo-1, and Centromere B. This modification to increase the current contract is necessary until a larger five (5) year requirement is competed and awarded. It is not in the Government's best interest to have a lapse prior to the larger requirement being awarded in 2016. The system and all of the components, shall be compliant with the Food and Drug Administration (FDA) requirements to market and deliver medical products for use in the United States of America, even should delivery be requested outside of the United States. The claims made for the product shall comply with the regulations of the FDA with respect to products for marketing and delivery of a medical product for use in the United States of America, even should delivery be requested outside of the United States. The equipment and reagents shall be compliance with OSHA requirements. Vendor shall be an Original Equipment Manufacturer (OEM) authorized dealer, authorized distributor or authorized reseller for the proposed equipment/system such that OEM warranty and service are provided and maintained by the OEM. All software licensing, warranty and service associated with the equipment/system shall be in accordance with the OEM terms and conditions. If a vendor challenges the basis of this sole source requirement, please email product capability statements (formats for submission: PDF, MS Word, or MS Excel) to Yun Hong at yun.p.hong.civ@mail.mil. Any challenges should reference number in the subject line: N62645-12-D-5053. Closing date for challenges is no later than 02:00 pm local time on 11 August 2016.
 
Web Link
FBO.gov Permalink
(https://www.fbo.gov/spg/DON/BUMED/N62645/N62645-12-D-5053/listing.html)
 
Place of Performance
Address: Naval Medical Center San Diego, San Diego, California, 92134, United States
Zip Code: 92134
 
Record
SN04200236-W 20160730/160728235226-230e70b704b8d2f9d2b3149e948720da (fbodaily.com)
 
Source
FedBizOpps Link to This Notice
(may not be valid after Archive Date)

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