COMMERCE BUSINESS DAILY ISSUE OF AUGUST 2,2000 PSA#2655 Department of Health and Human Services, Center for Disease Control and
Prevention, Procurement and Grants Office (Atlanta), 2920 Brandywine
Road, Room 3000, Atlanta, GA, 30341-4146 66 -- CHEMISTRY ANALYZER SOL 2000-N-00101 DUE 082900 POC William
Bancroft, Contract Specialist, Phone (770)488-2611, Fax (770)488-2670,
Email WBancroft@CDC.GOV -- Beth West, Procurement Technician, Phone
(770)488-2610, Fax (770)488-2670, Email BWest@CDC.GOV WEB: Visit this
URL for the latest information about this,
http://www2.eps.gov/cgi-bin/WebObjects/EPS?ACode=P&ProjID=2000-N-00101&LocID=2965. E-MAIL: William Bancroft, WBancroft@CDC.GOV. The Centers
for Disease Control and Prevention (CDC) intends to purchase a Roche
Boehringer Mannheim/Hitachi Model 912 Chemistry Analyzer. CDC believes
that its requirements are met only by this provider, however, all
responsible sources believing they can meet the specifications and
requirements listed herein may submit a proposal which will be
considered by the agency. Description of the requirements are: (1)
Analyzer must have minimum 90 manufacturer-supported methods (including
electrolytes by ion-selective electrodes (ISE), with 4-part reagent
configurations. All reagents must be packaged, sold, supported and
invoiced by the instrument manufacturer; (2) Analyzer must have 30 open
channels to allow use of methods/reagents by vendors other than Roche,
as well as user-developed chemistries; (3) Computer interface: must be
able to perform either in batch transmittal or real time, host query
mode. Must be able to interface with Local Area Network through RS-232
interface with software capable of directtransmission of ASCII file
upload of worklists with exact patient IDs created from barcoded
specimen label scanning off-line, and download of data containing those
patient IDs and accompanying results, analyte names, and dates and
times of analyses; (4) All reagents must have barcoding which tracks
lot number, calibration and control requirements and bottle size,
allowing automated calibration and quality control without operator
intervention; (5) Analyzer must be able to accommodate 5 different
samples types: serum/plasma, urine/spinal fluid, supernatant, and
"other."; (6) Analyzer must have the ability to pre-dilute,
post-dilute, or increase sample volume to accommodate repeat analysis
for confirmation of both low and high-concentration range samples. (7)
Analyzer must be able to process all urine methods, including
electrolytes from the collection vessel without operation intervention
or pre-dilution; (8) Analyzer must be able to automatically re-run
samples either before processing the next patient sample or at the end
of the run (with option selectable by the operator); (9) Instrument
must possess a separate refrigerated compartment for storage of all
calibrators and controls on-board. Instrument must also provide
refrigerated storage for up to 35 methods on-board, including
electrolytes; (10) All routine calibrators and controls must have
barcoded labels, to permit random positioning capabilities of these
materials; (11) Analyzer must provide the ability to quantitate the
amount of bilirubin, lipemia, and hemoglobin in patient samples
automatically and flag interference levels which can adversely affect
results; (12) Analyzer must have a minimum of three levels of software
access to instrument operating system; (13) Sampler area must have
ability to accept multiple tube sizes without adapters, as well as the
ability to accept multiple tube sizes consecutively; (14) Manufacturer
must offer own reagent systems for 17 serum proteins, including
C-reactive protein, in liquid, ready-to-use reagents; (15) Dimensions
should not exceed 42" wide x 32" deep x 40" high; (16) System must be
able to store 120 on-line reusable cuvettes, with manufacturer's
documentation that re-use is acceptable (i.e., cleaning protocol
ensures no contamination or carryover); (17) Computer system on-board
must be able to store 10,000 patient records and 5000 QC records before
older data must be deleted. Delivery must be made within 30 days of
contract award. THIS IS A COMBINED SYNOPSIS/SOLICITATION FOR COMMERCIAL
ITEMS PREPARED IN ACCORDANCE WITH FAR FORMAT PART 12.6, AS SUPPLEMENTED
WITH THE ADDITIONAL INFORMATION INCLUDED IN THIS NOTICE. THIS
ANNOUNCEMENT CONSTITUTES THE ONLY SOLICITATION; PROPOSALS ARE BEING
REQUESTED AND A WRITTEN SOLICITATION WILL NOT BE ISSUED. The following
provisions apply to this acquisition: FAR 52.212-1, Instructions to
Offerors -- Commercial Items; FAR 52.212-2, Evaluation -- Commercial
Items: the evaluation criteria stated in Paragraph (a) of this
provision are as follows: (1) technical capability of the proposed
system to meet the specifications stated herein, and (2) price. The
clause 52.212-4, Contract Terms and Conditions -- Commercial Items,
applies. The following FAR clauses are hereby added to this clause: FAR
52.211-16 (0% increase, 0% decrease, all items); FAR 52.247-35, FOB
Destination; The clause 52.212-5 Contract Terms and Conditions Required
to Implement Statutes or Executive Orders -- Commercial Items, applies
to this acquisition. The following clauses listed in paragraph (b) of
FAR 52.212-5 also apply: (7), (9), (10), (110), (14), (16), and (23).
Offerors shall include a completed copy of the provision at FAR
52.212-3, Offerors Representations and Certifications -- Commercial
Items, with proposal. This certification and documentation can be
obtained by downloading the FAR Clauses (Volume II) at
http://www.arnet.gov/far, and printing andexecuting the clauses
52.212-3 as indicated. This procurement is issued on an unrestricted
basis. Offerors shall use the Standard Form 1449,
"Solicitation/Contract/Order for Commercial Items" forms found at the
URL above. Offerors must show in their proposals (1) the Solicitation
number: 2000-N-00101; (2) Offeror's name, address and telephone number;
(3) A thorough, comprehensive description of the item being offered in
sufficient detail to permit evaluation of compliance with the
requirements of the solicitation; (5) Warranty terms; (6) Total price,
including all applicable costs; (7) Remit to address if different from
mailing address. The Government will award a contract resulting from
this solicitation to the responsible Offeror whose offer conforming to
the solicitation will be most advantageous to the Government. Offerors
are also advised that award may be made without discussions or any
contact concerning the proposal received. Delivery shall be made FOB
Destination within 30 days of contract award. Delivery and installation
shall be made to Centers for Disease Control and Prevention, National
Center for Environmental Health, Building 17 Loading Dock, 4770 Buford
Highway, N.E., Atlanta, GA 30341-3724. Payment terms are 80% upon
completion of installation and demonstration of compliance with
specifications, with remaining 20% to be paid 30 days later. Proposals
are due at 2:00 PM, August 29, 2000, to the following address: Centers
for Disease Control and Prevention, Procurement and Grants Office,
Attn: William Bancroft, Room 3220, 2920 Brandywine Road, Atlanta, GA
30341-4146. For information regarding the solicitation, contact Bill
Bancroft at (770) 488-2611. All responsible sources may submit an
offer. No telephone requests for the solicitation package can be
accepted. Posted 07/31/00 (D-SN480412). (0213) Loren Data Corp. http://www.ld.com (SYN# 0206 20000802\66-0005.SOL)
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