Automated Media Preparation Instrument for Dissolution Testing
Closed Pre-Solicitation Posted
- Solicitation number
- SSN_OC_2026_133856
- Agency
-
FDA Office of Acquisition and Grant Services
Food and Drug Administration, Department of Health and Human Services
- Responses due
- Set-aside
- Total Small Business
Opportunity facts
- NAICS code
- 334516 Analytical Laboratory Instrument Manufacturing
- Place of performance
- Irvine, California 92612, United States
- Points of contact
Notice details come from SAM.gov. Updated .
About this opportunity
The FDA Office of Acquisition and Grant Services anticipates procuring one Automated Media Preparation Instrument for Dissolution Testing via brand-name-or-equal acquisition, with responses to the sources sought notice due by May 10, 2026, and a formal solicitation anticipated shortly thereafter. This requirement carries a total small business set-aside.
Place of performance is the FDA Irvine Medical Products Laboratory in Irvine, California, with delivery required within 60 days of award and installation completed no later than 30 days after delivery.
The instrument must deliver volumes between 250ml and 1,000ml with dispensing accuracy of 5mL or less. In-line heating must reach at least 45°C with temperature accuracy of 2°C or better. The system must degas media to a maximum of 3.0ppm, remain compatible with media containing up to 2% surfactants, and feature an onboard controller capable of storing programmed methods and running in automatic or manual mode. The instrument must generate dispensing reports tracking volume and temperature, be portable with an included cart allowing filling of dissolution vessels in place on the apparatus, and operate on standard U.S. electrical outlets (115V, 50/60 Hz). Equipment must be newly manufactured, not refurbished or previously used for demonstration.
The reference standard for this brand-name-or-equal procurement is the Distek ezFill+ Dissolution Media Preparation Instrument. Award will be Firm-Fixed-Price for supply, delivery, installation, operator training, and one-year manufacturer's warranty. Responses to the sources sought notice should be directed to Reagan Davis, Contract Specialist, Reagan.Davis@fda.hhs.gov, and must include company information, CAGE Code, UEI, NAICS code, socio-economic status, relevant government contracts, domestic manufacturing status, and technical specifications.
Notice text
This requirement is being acquired as a brand-name-or-equal procurement. Equal products meeting all stated salient characteristics will be considered.
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- The instrument shall be capable of delivering a minimum volume of 250ml and a maximum volume of at least 1000ml.
- The instrument shall have a dispensing accuracy of ±5mL or less.
- The instrument shall be equipped with in-line heating that is capable of heating dissolution media to at least 45°C.
- The instrument shall have a temperature accuracy of ±2°C or better.
- The instrument shall be capable of degassing media up to a maximum of 3.0ppm.
- The instrument shall be compatible with media containing up to a maximum of 2% surfactants.
- The instrument shall have an onboard controller and user interface to select stored programs and set parameters for manual use.
- The instrument shall be capable of storing programmed methods and running in automatic or manual mode when preparing dissolution media.
- The instrument shall be capable of storing dispensing reports that include the volume and temperature dispensed.
- The instrument shall be portable with a cart or other mechanism, included, to allow the instrument to be moved to each dissolution instrument for use.
- The instrument shall be equipped with a dispensing nozzle that allows for dissolution vessels to be filled in place, while on the dissolution apparatus.
- Electrical requirement must be compatible with a standard US outlet, 115V, 50 or 60 Hz.
Safety Requirements
The Contractor shall ensure all equipment complies with applicable laboratory safety standards and manufacturer safety requirements. All installation activities shall be performed in accordance with applicable safety regulations to prevent hazards to personnel and facilities.
Trade and Service Specifications
- The instrument must be a newly manufactured unit, not used and refurbished or previously used for demonstration.
- FOB Point destination to include inside delivery and clean-up of area after installation.
- The entire system must be warranted for parts and labor for a minimum of 12 calendar months from the date of formal government acceptance. The vendor must also be capable of servicing the instrument through the covered warranty period. The system must include, at a minimum: coverage on all non-consumable items and parts supplied including base instrument, factory-certified replacement parts, engineer labor and travel costs. Any equipment repair and maintenance work shall be performed by an OEM-trained engineer. This factory-trained engineer shall have (verified by the OEM) the following: 1) access to OEM factory telephone support; 2) access to the most current OEM factory training for both hardware and software components; and 3) access to all current OEM factory parts, not build-to-order parts. The OEM-trained service engineer shall not use salvaged parts from other instruments for performing maintenance and repairs. All parts used in PM and repairs must be guaranteed, factory-tested, OEM quality parts.
- Instrument operators shall have access, for the duration of the 12-month warranty period, to a technical representative call center at no additional charge, for technical assistance and trouble-shooting, which is staffed by senior engineers to provide a high level of expertise for troubleshooting the instrument.
- Operator level training for 2 users at the delivery onsite location shall be provided at time of installation or shortly thereafter (within 30 days), such that operators are able to independently operate the instrument and included software to conduct routine analyses on the instrument.
- The Contractor shall provide installation by a trained and certified field service engineer who shall perform the necessary verification testing to demonstrate that the instrument meets the Original Equipment Manufacturer’s operational standards following installation. Consumables used for the installation shall be included.
Records and Reports
The Contractor shall, commensurate with the completion of each service call (inclusive of warranty service), provide the end-user of the equipment with a copy of a field service report/ticket identifying the equipment name, manufacturer, model number, and serial number of the equipment being serviced/repaired and detailing the reason for the service call, a detailed description of the work performed, the test instruments or other equipment used to affect the repair or otherwise perform the service, the name(s) and contact information of the technician who performed the repair/service, and for information purposes, the on-site hours expended and parts/components replaced. In addition, the Contractor shall provide monthly reports to the FDA Project Officer and Contract Specialist, not later that the 5th workday following the end of each month, summarizing all maintenance and repair activities (including warranty work) for the previous month (during months that work is performed).
Files
| File | Type | Posted |
|---|---|---|
| SSN.docx | DOCX document |
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