6550--Bio-Rad Quality Control Distributor to include Lot number standardization and Lot Sequester for VISN 16

Closed Pre-Solicitation Posted

Solicitation number
36C25624Q1112
Agency
Responses due
Set-aside
No set-aside

Opportunity facts

Notice details come from SAM.gov. Updated .

About this opportunity

Here is a two-paragraph summary of the key details from the Pre-solicitation notice:

The Department of Veterans Affairs, South Central VA Health Care System (VISN 16) has a requirement for an authorized distributor of Bio-Rad quality control (QC) materials to provide a wide range of Bio-Rad QC products with lot number standardization and lot sequestration management across the VISN 16 medical centers and outpatient clinics. The intent is to award a firm-fixed price Blanket Purchase Agreement (BPA) for a base year with four one-year option periods. Potential sources must demonstrate experience managing multi-facility QC programs, have valid distribution authorization from Bio-Rad, and meet specific inventory management and delivery requirements. Responses are due by July 19, 2024 and should include company details, relevant project experience, and capability to fulfill the stated requirements.

This procurement is not set-aside and the NAICS code is 325413 (In-Vitro Diagnostic Substance Manufacturing) with a small business size standard of 1,250 employees. No solicitation is currently available, and this notice is for market research purposes only with no guarantee of a future award. The government will not provide any feedback or compensation to respondents.

Notice text

THIS IS A SOURCES SOUGHT (MARKET SURVEY) NOTICE ONLY, NOT A SOLICITATION ANNOUNCEMENT AND SHOULD NOT BE CONSIDERED AS SUCH.

The Department of Veterans Affairs, South Central VA Health Care System (VISN 16) has a requirement for an authorized distributor of Bio-Rad® products to provide Bio-Rad ® Quality Control (QC) material to include VISN wide lot number standardization, lot sequester, and management for VISN 16 Medical Centers and Outpatient Clinic Laboratories. The intent of the projected RFQ is for the award of a firm-fixed price BPA (Blanket Purchase Agreement) for a base year (October 1, 2024 through September 30, 2025) plus 4 one-year options. VISN 16 locations are identified in Attachment A.

The Government will not pay for any information received in response to this notice, nor will the Government compensate any respondent for any cost incurred in developing the information provided to the Government. This notice does not constitute a commitment by the Government. Any information provided in response to this market survey will be used for informational purposes only and will not be released. Vendor participation is not a promise of future business with the Government. The purpose of this notice is to conduct market research and obtain information from qualified businesses.

Potential sources shall submit:

Business name, address, point of contact and phone number

Business size, any applicable socio-economic category, SAMS UEI and DUNS number

Information for recent/relevant projects equivalent in nature/size and complexity along with contract number(s),

Capability statement and product literature demonstrating ability to meet all of the requirements listed

Identification of company s GSA/Federal Supply Schedules (Group 65 VII)

Valid Vendor authorization letter of distribution for the required Bio-Rad Quality Control products signed by the manufacturer

The NAICS Code for this procurement is 325413, small business size standard is 1,250 employees.

Potential sources must demonstrate experience and knowledge of required products and capability to provide products and services.

Requirements:

The Contractor shall be responsible for assuring that an adequate supply of Bio-Rad quality control materials is available to meet the requirements. All participating V16 laboratories will be on the same lot of Bio-Rad control material at the same time. These items will be of the highest quality, sensitivity, specificity and tested to assure precision and accuracy. Following BPA award, unexpected changes in product will be at the expense of the contractor.

Potential sources shall also demonstrate in their response their abilities related to the following:

Contractor shall have a valid, signed Vendor authorization letter for distribution of the required Bio-Rad Quality Control products from the manufacturer.

Contractor shall provide Bio-Rad quality control materials, assayed and unassayed as delineated for each Bio-Rad product number and product name in Attachment A as described in their respective package inserts and listed in manufacturer s catalog.

Bio-Rad control materials shall include all analytes under the provided Bio-Rad product number and product name. Assayed control products with accompanying instrument specific ranges and target values shall be available for existing V16 chemistry/immunochemistry testing instrumentation.

Dedicated/designated staff assigned to manage the VISN 16 accounts ensuring BPA requirements are met.

Contractor shall assign a single individual to manage the VISN 16 standardized lot sequesters. The individual shall serve as the main point of contact for all communications regarding control products, inventories and sequestered products. Individual shall be experienced in managing multi-facility standardized sequesters of equivalent size and scope.

A second individual or team will be identified to serve as the back-up point of contact when the primary assigned individual is unavailable.

Contractor shall establish and sequester specific lots of the required Bio-Rad controls to ensure all ordering locations are using the same lot of controls at the same time for like products.

Contractor shall establish sequesters based on each respective laboratory test menu and workload in consideration of specific Bio-Rad control product stability, control frequency, lot expiration and availability of storage capacity within each lab at the required conditions.

Contractor shall offer maximized expiration dates for control lots to reduce frequency of new lot validations and/or parallel cross over studies for each laboratory.

Duration of each lot sequester shall also be maximized by the Contractor to reduce the number and frequency of lot changes and parallel studies for each laboratory.

Contractor shall appropriately and effectively manage inventories to prevent product waste.

Contractor may relocate product quantities within the network laboratories to enhance standardization of lot numbers at a given time. Concurrence shall be obtained from impacted laboratories prior to any adjustments. Adjustments shall not significantly reduce lot dating or create additional expense to the Government.

Contractor shall furnish monthly sequestered inventory updates by laboratory.

Contractor shall notify respective laboratories of removals/reductions of lot sequesters prior to monthly updates when significant changes occur and when sequestered quantities reach zero (0).

Contractor shall supply courtesy samples of upcoming lot of each control to sites prior to expiration or depletion of sequester inventory for performance of lot validations and/or parallel cross over studies. Shipment timing shall allow for completion of appropriate studies to meet accreditation requirements in adherence to individual lab policy/procedure.

Contractor shall provide recall notification, regardless of level, to each facility, and to the VISN 16 COR.

Medical Centers shall be notified immediately of any backorder item(s). Contractor s failure to provide any item, contained herein within the specified delivery time shall allow a Medical Center to obtain the product from another source.

Deliveries of BPA items shall be made the next business day (Tu-Fri) when orders are placed Monday -Thursday by the specified daily cut-off hour.

Deliveries shall be within regular work hours, which are usually 8:00 AM to 4:30 PM Central Time, Monday through Friday, for Medical Center Laboratories. Deliveries to Outpatient Clinic Laboratories shall be made during their hours of operation but no later than 30 minutes prior to daily close of business. Note: Hours may vary at different laboratories.

Required Bio-Rad Control Products:

Bio-Rad Item Number

Product Name

149

BIO-RAD CARDIAC MARKER LT LOW PLUS 1 LIQUID

182

BIO-RAD CARDIAC MARKER PLUS LEVEL 2 LIQUID

183

BIO-RAD CARDIAC MARKER PLUS LEVEL 3 LIQUID

361

BIO-RAD LIQUICHEK IA PLUS LEVEL 1

362

BIO-RAD LIQUICHEK IA PLUS LEVEL 2

363

BIO-RAD LIQUICHEK IA PLUS LEVEL 3

364

BIO-RAD SPECIALTY IA LIQUID LEVEL 1

365

BIO-RAD SPECIALTY IA LIQUID LEVEL 2

366

BIO-RAD SPECIALTY IA LIQUID LEVEL 3

383

BIO-RAD LIQUICHEK Serum Volatile LEVEL 1

384

BIO-RAD LIQUICHEK Serum Volatile LEVEL 2

397

BIO-RAD LIQUICHEK URINE CHEM LEVEL 1

398

BIO-RAD LIQUICHEK URINE CHEM LEVEL 2

423

BIO-RAD URINE TOX S1E LOW OP LIQUID

424

BIO-RAD URINE TOX S2E LOW OPLIQUID

460

BIO-RAD URINE TOX NEGATIVE LIQUID

514

BIO-RAD LIQUICHEK SED RATE LEVEL 1

515

BIO-RAD LIQUICHEK SED RATE LEVEL 2

544

BIO-RAD LIQUICHEK ETH/AMM LEVEL 1

545

BIO-RAD LIQUICHEK ETH/AMM LEVEL 2

546

BIO-RAD LIQUICHEK ETH/AMM LEVEL 3

547

BIO-RAD TUMOR MARKER, Level 1 LIQUID

549

BIO-RAD TUMOR MARKER, Level 3 LIQUID

594

BIO-RAD LIQUICHEK IMMUNOLOGY LEVEL 1

596

BIO-RAD LIQUICHEK IMMUNOLOGY LEVEL 3

683

BIO-RAD S1O LOW OPIATE

697

BIO-RAD MULTIQUAL UNASSAYED LEVEL 1 LIQUID

699

BIO-RAD MULTIQUAL UNASSAYED LEVEL 3 LIQUID

751

BIO-RAD LIQUICHEK SPINE FLUID LEVEL 1

752

BIO-RAD LIQUICHEK SPINE FLUID LEVEL 2

12001084

BIO-RAD Liquichek Cardiac Troponin Control Level 1Â Â

12006239

BIO-RAD Liquichek Cardiac Troponin Control Level 2Â

12006369

BIO-RAD Liquichek Cardiac Troponin Control Level 3Â

27124

BIO-RAD Lyphochek Specialty IA Level 1

27125

BIO-RAD Lyphochek Specialty IA Level 2

27126

BIO-RAD Lyphochek Specialty IA Level 3

12011343

BIO-RAD DIABETES Level 1 LIQUID

12011345

BIO-RAD DIABETES Level 3 LIQUID

12000404

BIO-RAD LIQUICHEK Whole Blood Immunosuppressant Level 1

12000405

BIO-RAD LIQUICHEK Whole Blood Immunosuppressant Level 2

12000406

BIO-RAD LIQUICHEK Whole Blood Immunosuppressant Level 3

12000407

BIO-RAD LIQUICHEK Whole Blood Immunosuppressant Level 4

12005787

BIO-RAD LIQUICHEK OPIATE CONTROL Level 2

12012693

BIO-RAD Liquichek Serum Indices Level Hemolysis

12012694

BIO-RAD Liquichek Serum Indices Level Icterus

12012695

BIO-RAD Liquichek Serum Indices Level Lipemia

12012696

BIO-RAD Liquichek Serum Indices Level Non-Interfered

A list of required Bio-Rad control products by product number and annual estimated usage by laboratory are provided in Attachment A.

Potential sources are to respond by email only to the Contracting Officer, Tammie Chaney at tammie.chaney@va.gov no later than 1:00pm CST on July 19, 2024. Include the following in the email subject line: RFI - Bio-Rad QC Products . Questions or inquiries will not be answered or acknowledged, and no feedback will be provided. No vendor will be provided information on solicitations issued on a Government Point of Entry based on this sources sought notice.

This notice is to assist in determining sources only. There is no solicitation currently available. There is no guarantee, expressed or implicit, that the market research for this acquisition will result in a particular set-aside, sole source award or any other guarantee of award strategy. All information is to be provided on a voluntary basis and at no charge to the Government.

DISCLAIMER: This notice is issued solely for informational and planning purposes and does not constitute a solicitation. Responses to this notice are not offers and cannot be accepted by the Department of Veterans Affairs to form a binding contract. Respondents are solely responsible for all expenses associated with responding to this notice.

Files

File Type Posted
Attach A BR QC.xlsx XLSX spreadsheet
36C25624Q1112.docx DOCX document

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