6550--immunology testing supplies

THIS REQUEST FOR INFORMATION (RFI) IS ISSUED SOLELY FOR INFORMATION AND PLANNING PURPOSES ONLY AND DOES NOT CONSTITUTE A SOLICITATION.

THE SUBMISSION OF PRICING, CAPABILITIES FOR PLANNING PURPOSES, AND OTHER MARKET INFORMATION IS HIGHLY ENCOURAGED AND ALLOWED UNDER THIS RFI IN ACCORDANCE WITH (IAW) FAR 15.201(e).

DISCLAIMER

This RFI is issued solely for information and planning purposes only and does not constitute a solicitation. All information received in response to this RFI that is marked as proprietary will be handled accordingly. IAW FAR 15.201(e), responses to this notice are not offers and cannot be accepted by the Government to form a binding contract. Responders are solely responsible for all expenses associated with responding to this RFI.

SOURCES SOUGHT DESCRIPTION

This is NOT a solicitation announcement. This is a RFI only. The purpose of this RFI is to gain knowledge of potential qualified sources and their size classification relative to NAICS 325413 (size standard of 1250 Employees). Responses to this RFI will be used by the Government to make appropriate acquisition decisions. After review of the responses to this RFI, a solicitation announcement may be published. Responses to this RFI synopsis are not considered adequate responses for a solicitation announcement.

The Department of Veterans Affairs (VA), VISN 22 Network Contracting Office, is seeking sources that can provide Immunology Testing Supplies that at a minimum meets the following salient characteristics with a brand name or equal product for the VA Tucson Healthcare System:

The reagents, consumables and supplies must be approved for use with Bio-Rad s, BioPlex 2200.

All supplies, reagents, controls, calibration materials, disposables, and any consumable parts necessary for analyzer operation, must be Food and Drug Administration (FDA) approved.

The quality control results generated from all tests performed with BioPlex 2200 must be compatible with Unity Real Time software.

The vendor must generate and provide monthly evaluations with the following reports:

Laboratory Performance Overview

Laboratory Comparison Report

Laboratory Histogram

To secure continuity between lots of reagents and consumables the vendor should be able to directly sequester reagents and consumables from the lots currently being used.

The vendor must directly distribute all requested products no more than 2 days after receipt or order (ARO).

The vendor must send monthly updated reserve reports of sequestered quality control

Brand name Info:

BRAND

PRODUCT DESCRIPTION

PRODUCT #

QTY

Bio-Rad

D-100 CPR Billing

19000041

54000

Bio-Rad

Analytical Cartridge/Calibrator Pack

2901004

1

Bio-Rad

Prefilter (5 per package)

2901007

1

Bio-Rad

Elution Buffer A

2901010

9

Bio-Rad

Elution Buffer B

2901011

3

Bio-Rad

Wash Solution

2901012

9

Bio-Rad

Sample Diluent

2901009

3

Bio-Rad

D-100 Microvials (100 per package)

12000243

3

Bio-Rad

Calibrator Pack

2901006

1

Bio-Rad

Cleaning Tube

2901008

1

The information identified above is intended to be descriptive, not restrictive and to indicate the quality of the supplies that will be satisfactory. It is the responsibility of the interested source to demonstrate to the government that the interested parties can provide the supplies/services that fulfill the required specifications.

If you are interested and are capable of providing the sought-out supplies, please provide the requested information as well as the information indicated below. Response to this notice should include company name, address, point of contact, size of business pursuant to the following questions:

(1) Please indicate the size status and representations of your business, such as but not limited to: Service-Disabled Veteran Owned Small Business (SDVOSB), Veteran Owned Small Business (VOSB), HUBZone, Woman Owned Small Business (WOSB), Large Business, etc.)?

(2) Is your company considered small under the NAICS code identified under this RFI?

(3) Are you the manufacturer or distributor of the items being referenced above (or equivalent product/solution)? What is the manufacturing country of origin of these items?

(4) If you re a small business and you are an authorized distributor/reseller for the items identified above (or equivalent product/solution), do you alter; assemble; modify; the items requested in any way? If you do, state how and what is altered; assembled; modified?

(5) Does your company have an FSS contract with GSA or the NAC or are you a contract holder with NASA SEWP or any other federal contract? If so, please provide the contract type and number.

(6) If you are an FSS GSA/NAC or NASA SEWP contract holder or other federal contract holder, are the referenced items/solutions available on your schedule/contract?

(7) Please provide general pricing for your products/solutions for market research purposes.

(8) Please submit your capabilities in regards to the salient characteristics being provided and any information pertaining to equal to items to establish capabilities for planning purposes?

*** Submissions addressing Section (8) should show clear, compelling and convincing*** evidence that all equal to items" meet all required salient characteristics.

Responses to this notice shall be submitted via email to kahlfanie.carabon@gov. Telephone responses shall not be accepted. Responses must be received no later than Thursday, November 21st, 2024 at 1:00 P.M. Pacific Time. If a solicitation is issued it shall be announced at a later date, and all interested parties must respond to that solicitation announcement separately from the responses to this request for information. Responses to this notice are not a request to be added to a prospective bidders list or to receive a copy of the solicitation.

Notice: No remanufactured or gray market items/supplies will be acceptable. Interested parties of RFI must be an authorized reseller, distributor, or dealer of the Original Equipment Manufacturer (OEM). Verification can be provided by an authorization letter or other documents from the OEM. Equipment shall be in accordance with the OEM terms and conditions.