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Single-Axis Linear Motion Calibration System (Shake Table) with Control Software

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SSN-CDRH-2026-133952Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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The U.S. Food and Drug Administration is seeking market information for a single-axis linear motion calibration system, commonly known as a shake table, with integrated control software, to be used for laboratory calibration and testing of inertial measurement devices. The system must deliver programmable, closed-loop linear motion with real-time feedback, supporting arbitrary user-defined waveforms including at least three simultaneous frequency components, operating within a frequency range of 0.1 to 10 Hz, displacement of sub-millimeter to twenty millimeters, and acceleration up to approximately one g, with sub-millimeter positioning accuracy. It must include factory-calibrated NIST-traceable position and reference accelerometer sensors, safety mechanisms such as hard-wired emergency stop and automatic shutdown, and a benchtop design compatible with standard 110–120V power. The accompanying control software must operate offline without cloud dependencies, support programming interfaces like MATLAB or Python, allow non-proprietary data exchange, and comply with Section 508 accessibility standards. The system must be delivered fully assembled, factory-tested, and calibrated, with installation, user training, technical documentation, and a commercial warranty included, and must be delivered to the FDA White Oak campus in Silver Spring, Maryland, within 90 days of award. This is a sources sought notice for market research only and does not constitute a binding solicitation or obligation to procure. Responses must include a completed Vendor Response Form in native Microsoft Excel format and a five-page capability statement in PDF, both submitted via email to Reagan Davis by August 3, 2026. Respondents are required to declare their business size under NAICS 334519, identify socioeconomic classifications, indicate whether they are manufacturer, distributor, or reseller, and specify if supplying U.S.-made end products consistent with the Buy American Act and nonmanufacturer rule. All respondents must disclose the country of manufacture, domestic content percentage, origin of critical components, production capacity, and whether alternatives or substitutes exist domestically. The Government will use this information to determine market availability, assess potential for small business set-asides, and evaluate domestic production feasibility, and responses must not include proprietary pricing. No payment will be made for response costs, and failure to respond does not preclude future participation if a solicitation is issued.

General Info

FDA seeks market info for benchtop shake table with NIST-traceable sensors, offline software, 0.1–10 Hz range, sub-mm accuracy, delivered to Silver Spring in 90 days.

Agency

Department Of Health And Human Services → FDA Office Of Acq Grant SvcsView Agency

NAICS

334519 - Other Measuring and Controlling Device ManufacturingView NAICS

Place of Performance

Silver Spring, MD, 20993, USA

Set-Aside

NONE

Documents

(1)

CDRH-2026-133952+SSN+Vendor+Response.xlsx

XLSX

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → FDA Office Of Acq Grant Svcs
Contacts1 person available
OfficeRockville, MD, 20852, USA
Organization / Agency
Department Of Health And Human Services → FDA Office Of Acq Grant Svcs
View Agency Profile
Office AddressRockville, MD, 20852, USA

Full Description

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NOTICE ID: CDRH-2026-133952


SOURCES SOUGHT NOTICE: Single-Axis Linear Motion Calibration System (Shake Table) with Control Software


NAICS / Size Standard: 334519 / 600 employees | PSC: 6635 — Physical Properties Testing and Inspection | Place of Delivery: FDA White Oak, Silver Spring, MD


Responses due: See SAM.gov posting and submit by email to Reagan Davis, Reagan.Davis@fda.hhs.gov.


1.0 PURPOSE AND DISCLAIMER


THIS IS A SOURCES SOUGHT NOTICE ONLY, issued for market research under RFO Part 10. It is not a solicitation and does not commit the Government to issue one. The Government will not pay any costs incurred in responding. Responses will not be returned and respondents will not be notified of results. Not responding does not preclude participation in any future solicitation, which, if issued, will be posted to SAM.gov.


This notice has two purposes: (1) to identify sources of any business size capable of supplying domestic end products meeting this requirement, in support of the Government's obligations under the Buy American statute and RFO Part 25; and (2) to determine whether capable small business concerns, whether as manufacturer, OEM, authorized distributor, or reseller, exist in sufficient number to support a set-aside under RFO Part 19. Responses will inform the acquisition strategy, including the set-aside decision and any domestic availability determination, and may be summarized in market research documentation posted publicly with a proposed nonavailability waiver, if applicable. Do not submit proprietary pricing; mark any confidential business information clearly.


2.0 DESCRIPTION OF REQUIREMENT


The U.S. Food and Drug Administration requires one (1) complete, turnkey single-axis (one degree-of-freedom) linear motion calibration system, commonly described as a shake table, with control software, for laboratory calibration, verification, and validation testing of inertial measurement devices. The system shall be fully assembled, factory-tested, and factory-calibrated prior to shipment, requiring only unpacking, cable connection, and software installation by the end user.

The Government seeks sources able to provide a system meeting, at minimum, the following salient performance characteristics. These are stated in approximate terms for market research; the full minimum specification will accompany any resulting solicitation.
•  Programmable single-axis linear motion under closed-loop position control with real-time feedback, capable of arbitrary user-defined waveforms including multi-frequency superposition of at least three simultaneous components. Pre-programmed, fixed-routine-only calibrators are not sought.
•  A motion envelope on the order of 0.1 to 10 Hz in frequency, sub-millimeter to approximately twenty millimeters in displacement, and up to approximately one g in acceleration, with demonstrated small-amplitude positioning accuracy at the sub-millimeter level.
•  An integrated position sensor and an integrated reference accelerometer, each factory calibrated with NIST-traceable certificates.
•  Safety features including a hard-wired emergency stop, motion limits, over-current protection, and fault detection with automatic safe shutdown.
•  Benchtop form factor suitable for standard laboratory power (110 to 120V, or universal input) without special power conditioning or floor reinforcement.
•  Control software operable in a standalone configuration with no required internet, cloud, or subscription, a programmable interface compatible with MATLAB, Python, or an equivalent industry-standard environment, and non-proprietary data import and export.
•  Software and electronic content conforming to Section 508 accessibility standards, supported by a Voluntary Product Accessibility Template or equivalent.

Estimated quantity: one (1) each. Anticipated delivery: within approximately 90 days after award. Place of delivery: FDA White Oak campus, Silver Spring, Maryland. Applicable standards: NIST-traceable calibration; Section 508. Installation, user training, technical documentation, and a commercial warranty are included in the anticipated requirement.


3.0 INSTRUCTIONS TO RESPONDENTS


Responses shall be submitted by email to the point of contact identified in the SAM.gov posting no later than the response due date, with subject line “Sources Sought Response – CDRH-2026-133952 - [COMPANY NAME].” A complete response consists of:


(a) The Vendor Response Form (Attachment 1), completed and returned in its NATIVE MICROSOFT EXCEL (.xlsx) FORMAT. Do not convert the form to PDF, scan it, or alter its structure. Name the file: CDRH-2026-133952_CompanyName.xlsx; and


(b) A capability statement not exceeding five (5) pages in PDF format providing narrative elaboration and supporting documentation as applicable (product literature, specification sheets, letters of supply or authorized distribution).


The Company Information fields in Section 4.0 and the questions in Sections 5.0 and 6.0 below are reproduced in the Vendor Response Form. The Government intends to consolidate and analyze market data directly from the returned forms; responses submitted without the completed form in native Excel format may not be fully considered in the Government’s analysis. Telephone inquiries will not be accepted.


4.0 COMPANY INFORMATION (provide all of the following)


4.1. Company Name / Address:


4.2. UEI / CAGE Code:


4.3. Point of Contact (Name, Phone, Email):


4.4. Active SAM.gov Registration (Yes/No):


4.5. Business Size under the stated NAICS (Small / Other than Small):


4.6. Socioeconomic Categories (all that apply): 8(a); HUBZone; SDVOSB; VOSB; WOSB; EDWOSB; SDB; None


4.7. Existing Contract Vehicles (FSS/MAS, GWAC, IDIQ/BPA):


5.0 SMALL BUSINESS CAPABILITY QUESTIONS


5.1. Identify your role for the required items: OEM, manufacturer, authorized distributor or dealer, reseller, or other (describe). If a distributor or reseller, identify the manufacturer(s) of the end items you would supply and provide evidence of authorized distribution, if available.


5.2. If you are a small business that is not the manufacturer of the end item, state whether you can supply end items manufactured by a small business concern in the United States, consistent with the nonmanufacturer rule (13 CFR 121.406), and identify that manufacturer if known. If you would supply the product of an other than small or foreign manufacturer, state this clearly.


5.3. Describe your capability and capacity to fulfill the full scope of this requirement, including the quantities and delivery timeframes in Section 2.0, and identify any portion you could not fulfill. Include relevant experience (up to three recent contracts or commercial sales) and any applicable quality or regulatory certifications. Federal experience is not required.


5.4. Describe any teaming, joint venture, or subcontracting arrangements you anticipate.


6.0 DOMESTIC MANUFACTURE AND AVAILABILITY QUESTIONS


All respondents shall answer, regardless of business size.


6.1. Identify the country (or countries) in which the offered end item is manufactured and the operations performed at each location.


6.2. If manufactured in the United States, state whether the item meets the domestic content threshold in effect under RFO 25.101 as of the anticipated award date, or the approximate domestic content percentage you can certify to. State whether the item is a commercially available off-the-shelf (COTS) item and whether it consists wholly or predominantly of iron or steel.


6.3. Identify the country of origin of any critical components or components for which no domestic source is known to you.


6.4. If you can supply a domestic end product, describe production capacity against the Section 2.0 quantities (sustainable output, available inventory, lead times). If you can satisfy the requirement only in part (insufficient quantity) or with deviations from the salient characteristics (insufficient quality), describe the shortfall specifically.


6.5. If you do not currently manufacture a domestic end product meeting this requirement, state whether and under what conditions you could establish or expand domestic production (estimated timeline, minimum quantities, or other commitments required).


6.6. Identify any alternative or substitute items manufactured in the United States that could satisfy the Section 2.0 characteristics, including items made by other firms, and any other known domestic manufacturers or supply chain constraints relevant to domestic availability.

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New
Federal
Proficiency Testing ContractThe U.S. Food and Drug Administration intends to award a sole-source, firm-fixed-price order to QuoData GmbH of Dresden, Germany, for the continued support and specialized enhancements of the ProLab Plus software platform, which is exclusively used to analyze proficiency testing and inter-laboratory study data. The contract, issued under FAR 6.103-1, justifies noncompetitive procurement because QuoData is the sole provider of this proprietary software, which is essential to the FDA’s Human Foods Program for evaluating laboratory performance and supporting accreditation. Market research confirms no alternative solutions exist that can meet the technical requirements, particularly the need for advanced statistical methodologies aligned with ISO standards, which require direct expertise from the original developer beyond standard technical support. The contract structure includes a one-year base period followed by four optional one-year extensions, with a total potential duration of five years. The North American Industry Classification System code is 541611 for Administrative Management and General Management Consulting Services. The order will be performed from Silver Spring, Maryland, with procurement managed by the FDA Office of Acquisition and Grant Services based in Rockville, Maryland. Interested parties may submit inquiries by the response deadline of August 4, 2026, but this presolicitation notice does not constitute a request for competitive proposals. Primary and secondary points of contact have been designated for further information regarding the procurement.
Administrative Management and General Management Consulting Services

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NAICS: 61143
New
Federal
Generic Drug Pathway Curriculum: From ANDA Submission to Global RelianceThe U.S. Food and Drug Administration’s Office of Acquisitions and Grants Services is conducting market research to identify qualified vendors capable of delivering the Global Abbreviated New Drug Application (ANDA) Training Program, with a focus on developing and delivering a comprehensive curriculum covering the generic drug pathway from ANDA submission to global reliance. This notice is strictly a sources sought announcement under FAR Part 10, meant solely for planning and market intelligence purposes, and does not constitute a solicitation, commitment, or obligation to award a contract or compensate respondents. The anticipated contract, if pursued, would have a five-year performance period from September 15, 2026, through September 14, 2031, including a base year and four optional years. Interested parties are requested to submit a completed Vendor Feedback Form, tracked comments on the Draft Statement of Work and Draft Global ANDA Training - Generic Drug Curriculum in MS Word format, and a Capability Statement, all sent via email to Lawrence Edelmann by 12:00 p.m. Eastern Time on July 28, 2026. Responses will inform the development of a potential future solicitation, and the government reserves the right to follow up with respondents for additional details without providing feedback to all submitters. The NAICS code associated with this effort is 61143, and the primary point of contact is located at the FDA’s office in Rockville, Maryland, with performance expected in Silver Spring, Maryland.

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