Blood Plasma Spray Drying System

Active

Contract Opportunity

Request for Information (RFI)

1. RFI Number: HT9425-25-R-JLM002

2. RFI Title: Blood Plasma Spray Drying System for US Army Institute of Surgical Research (USAISR).

3. Agency: United States Army Medical Research and Development Command (USAMRDC)

4. Office: United States Army Institute of Surgical Research (USAISR)

5. Contracting Office: United States Army Medical Research Acquisition Activity (USAMRAA), Fort Detrick, Frederick, MD.

6. Location: Fort Detrick, MD

7. Synopsis: This RFI is for information and planning purposes only, at this time, and shall not be construed as a Request for Quote (RFQ) or obligation on the part of the USAMRDC. This RFI is not expected to be a RFQ or Invitation for Bid, nor does it restrict the Government to an ultimate acquisition approach. This notice is for information and planning purposes only, and is not to be construed as a commitment by the Government. The Government will not pay for solicited information. At this time, no RFQ exists; therefore, please do not request a copy of the RFQ. Telephonic inquiries will not be accepted. If an RFQ is released, a synopsis will be posted in sam.gov. It is the responsibility of any potential vendor to monitor the sam.gov website for the release of any RFQ or synopsis.

8. Background: The United States Army Institute of Surgical Research (USAISR) is part of the U.S. Army Medical Research and Development Command (USAMRDC). The USAISR is dedicated to both laboratory and clinical trauma research. Its mission is to provide requirements-driven combat casualty care medical solutions and products for injured soldiers from self-aid through definitive care across the full spectrum of military operations; provide state-of-the-art trauma, bum, and critical care to Department of Defense (DoD) beneficiaries around the world and civilians in our trauma region; and provide Burn Special Medical Augmentation Response Teams.

9. Objective and Purpose:

The Technical Requirements / Minimum Essential Characteristics (MECs) are as follows:

The USAISR seeks a blood plasma spray drying system that can be used for clinical transfusion purposes. The USAISR is seeking a spray dryer, a sealer and the plastic consumable components that are sterile-docked to blood plasma bags in a completely closed, aseptic process. The system should be able to produce a dried plasma product in bag suitable for transfusions. The system will need to be able to produce a product suitable for clinical transfusions without the need for a sterile room. System should be able to produce a spray dried unit of plasma greater than or equal to 48g.

1. Modular equipment with no more than 3 separate units (Dyer, Sealer, Clean Dry Air System).


2. Dying Modular Unit Specifications
   
   
   
   1. Equipment should have dimensions equal to or smaller than 32x25.2x77.5 (DxWxH) inches.
   
   
   2. The weight of the equipment should be less than 560 pounds.
   
   
   3. The electrical requirement should be 208VAC at 60hz and 30amps.
   
   
   4. Equipment should utilize an L6-30P connector.
   
   
   5. Unit should have an air flow of at least 800 SLPM (Standard Liters Per Minute).
   
   
   6. The operating pressure should be between 90-120 pounds per square inch (psi).
   
   
   7. Equipment should have a dedicated exhaust.
   
   
   8. Equipment should be capable of operating in 15-40˚ C temperatures with relative humidity less than or equal to 75%.
   
   
   9. The safe operating altitude should be between sea level and 6,750 feet.
   
   
   10. The recommended operating pressure should be between 0.95-1.05 atmospheres.
   
   
   11. The recommended operating noise should equal to or less than 65 decibels.
   
   
   12. Should operate with an integrated, simple user interface
   
   
   
   


3. Sealing Modular Unit Specifications
   
   
   
   1. The sealing modular unit should have dimensions equal to or less than 34.7x29.3x77 (DxWxH) inches.
   
   
   2. The weight of the equipment should be between less than 550 pounds.
   
   
   3. The voltage of the equipment should be 208VAC at 60hz and 20amps.
   
   
   4. The equipment should utilize a L6-30P connection for electricity.
   
   
   5. The air requirements for the devices should be 90-105psi and it should utilize a quick disconnect adaptor.
   
   
   6. Equipment should be capable of operating in 15-40˚ C temperatures with relative humidity less than or equal to 75%.
   
   
   7. The safe operating altitude should be between sea level and 6,750 feet.
   
   
   8. The recommended operating pressure should be between 0.95-1.05 atmospheres.
   
   
   9. The recommended operating noise should equal to or less than 70 decibels.
   
   
   
   


4. Utilizes a clean Dry Air System
   
   
   
   1. Oil-free air compressor.
   
   
   2. desiccant dryer.
   
   
   3. air-tank.
   
   
   4. and ancillary filters.
   
   
   
   


5. Utilizes single-use consumables.
   
   
   
   1. Equipment should come with 50 to 470 units of plasma drying chambers.
   
   
   2. Equipment should come with 50 to 470 units of plasma pretreatment containers.
   
   
   3. Equipment should come with 50 to 470 units of sterile water for injection.
   
   
   4. Equipment should come with 50 to 470 units of transfer sets.
   
   
   5. Equipment should come with 50 to 470 units of packing including desiccant.
   
   
   
   

10. Information Requested in Capability Statement:

Provide information on the ability to provide Blood Plasma Spray Drying System as listed above.

11. North American Industry Classification System (NAICS) Code: The NAICS code for this potential action is 334519 – Other Measuring and Controlling Device Manufacturing.

12. Response Due Date: Interested parties should submit the attached RFI response electronically by 12:00 pm Eastern 17 February 2025 via e-mail to Jeremy McMurry at Jeremy.l.mcmurry.civ@health.mil

13. Instructions to Responders:

13.1 The Government appreciates responses from all capable and qualified sources.

13.2 The subject header of the e-mail for submission of questions and/or the RFI response shall be: HT9425-25-R-JLM002.

13.3 Interested firms should submit a response (Capability Statement) that demonstrates the Offeror’s capabilities as they relate to the requirements identified in this RFI. The Capability Statement shall not exceed three (3) typed pages; additional sheets for cover page will not be counted toward page limitation.

13.3.1

a. Cover Page (1 page)

i. Title

ii. Organization

iii. Responders technical and administrative points of contact (names, addresses, phone, fax number and email addresses)

b. Current Technical Expertise, Knowledge, and Product Availability

i. Discussion of capabilities/challenges/technologies

ii. Technical response, demonstrate the ability to provide: Blood Plasma Spray Drying System

c. Brief summary of relevant experience pertaining to the requirement (for example: government, academia, or industry experience).

13.4 Provide the below information when responding to this Sources Sought / RFI.

RFI Number

Company Name

Company Address

Point of Contact

Phone Number

E-mail Address

Tax Identification Number (TIN)

Cage Code

Unique Entity Identifier

Company Web Page

Company Location(s)

Company is / is not a Small Business

Company is / is not SAM Registered

Other Classifications (e.g. 8(a), HubZone, Woman-Owned, Veteran-Owned, Service-Disabled Veteran-Owned)

14. Disclaimer and Important Notes: The purpose of this RFI notice is to gain market knowledge. The Government is not obligated to award a contract or otherwise pay for the information provided in the responses received. The Government reserves the right to use information provided by respondents for any purpose deemed necessary and legally appropriate. Any organization responding to this notice should ensure that its responses are complete and sufficiently detailed to allow the Government to determine the organization's solution. Responders are advised that the Government is under no obligation to acknowledge receipt of the information received, or to provide feedback to respondents regarding any information submitted. After a review of the responses received, a RFQ may be published in sam.gov. Responses to this notice will not be considered adequate responses to an RFQ.

15. Confidentiality: No proprietary, classified, confidential, or sensitive information should be included in submitted responses. The Government reserves the right to use any non-proprietary technical information in any resultant RFQ(s).

Original Point of Contact

POC: Jeremy McMurry, Jeremy.l.mcmurry.civ@health.mil

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