Active Solicitation · DEPARTMENT OF VETERANS AFFAIRS

    Q301--Cleanroom Testing SB Set-Aside Solicitation

    DEPARTMENT OF VETERANS AFFAIRS
    Sol. 36C26326Q0571SolicitationSaint Paul, MN
    Open · 5d remaining
    DAYS TO CLOSE
    5
    closes Apr 28, 2026
    POSTED
    Apr 23, 2026
    Publication date
    NAICS CODE
    541380
    Primary industry classification
    PSC CODE
    Q301
    Product & service classification

    AI Summary

    The Department of Veterans Affairs is soliciting proposals for cleanroom testing services, including glove and fingertip testing, media fill kits, and incubation of samples. Bidders must provide pricing per plate, including shipping, and adhere to specific reporting requirements. This opportunity is set aside for small businesses and does not fall under Simplified Acquisition Procedures.

    Contract details

    Solicitation No.
    36C26326Q0571
    Notice Type
    Solicitation
    Posted Date
    April 23, 2026
    Response Deadline
    April 28, 2026
    NAICS Code
    541380AI guide
    PSC / Class Code
    Q301
    Contract Code
    3600
    Primary Contact
    Joseph A Bloomer
    State
    MN
    ZIP Code
    55101
    AI Product/Service
    service

    Award information

    Awardee
    null
    Award Date

    Description

    Cleanroom Testing Q&A CLIN 0001- what is included in this Clin?  It is for glove/fingertip testing post gowning and garbing plates? Does this include the plates for post media fill glove/fingertip and post media fill surface sample? This includes post garbing glove fingertips, post media fill glove fingertips, and the post media fill surface. Price would be a per plate price to include shipping plates to facility and incubation of plates. Historically, EMSL has provided the media plates FREE of charge à (100mm for glove fingertips, 55mm for surface sampling post media fill test and routine monthly surface & semi-annual air testing. The VA has paid for the shipping of plates to the outside lab for incubation.  CLIN 0004- Media fill kits Price would be for incubation only as VA will supply own media fill kits. Identification charged separately under CLIN 0005. VA supplies own media fill kits. Media is read as turbid or turbidity is absent. There is NO identification of organisms in a failed media fill bag. Page 9 of 70, provided by the contractor free of charge with no limit on the number of plates pursuant to this contract including cost of shipping the plates a. This implies that the cost of plates and shipping is to be included in the relevant CLIN(s) to cover this cost, but to avoid losing money while still submitting a competitive offer, can you clarify if the number of required plates could exceed the CLIN quantities? Estimate approximately 10-15 % of the plates we receive are wasted due to damage / mishandling / excessive condensation, etc. Estimate numbers should be fairly accurate but if there is a need for additional plates, a modification would need to be submitted to add any additional plates above the submitted numbers. Page 13 of 70, contractor will report the starting temperature for each interval of incubation, dates of incubation, and the identification of the person who reads and documents the results . a. Is it sufficient that the laboratory report includes the names of technicians who conducted work on the samples in a general sense, Or b. Does the VA require that specific personnel be explicitly identified for each individual activity (e.g., incubation setup, incubation interval monitoring, reading of results, and documentation/reporting) throughout the report? It is not specifically required to identify individual personnel for each distinct activity throughout the incubation / analysis process. The final report must include a signature from an authorized signatory, such as a microbiology laboratory manager or another approved individual. Page 17 of 70, Must contain the following information 100% of the time: 10) Preliminary cfu counts after initial incubation . Specifically, we would like to confirm whether this requirement is intended to apply universally to all samples, or if there is flexibility in how preliminary data are reported. Is it required that preliminary CFU counts after initial incubation be included in all reports (100% of the time), or Would it be acceptable to provide preliminary CFU counts in a Preliminary Report only in cases where results indicate potential ISO/action level failures, with the Final Report containing the confirmed total bacterial CFU and total fungal CFU following full incubation? It is acceptable to issue a preliminary report only when initial results suggest an exceed action level in USP<797>. The final report must include both the preliminary results and the confirmed final counts for bacterial and fungal CFUs, alongside organism identification for any samples that exceed action levels as defined in USP 797."

    Key dates

    1. April 23, 2026Posted Date
    2. April 28, 2026Proposals / Responses Due

    AI search tags

    Frequently asked questions

    Q301--Cleanroom Testing SB Set-Aside Solicitation is a federal contract award from DEPARTMENT OF VETERANS AFFAIRS. Review the award details including the awardee, contract value, and NAICS code.

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