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This Pre-Solicitation opportunity from Department Of Defense was posted on March 25, 2009. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Robotic Dispensing System

Closed
N0001809RCB01Y9Federal

Contract Overview

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General Info

NAICS

339112 - Surgical and Medical Instrument Manufacturing

Place of Performance

Branch Medical Clinic Belle Chasse BLDG 41, 400 Russel St, BELLE CHASSE, LA, 70143, USA

Set-Aside

NONE

Documents

0

No documents available

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Timeline

PhaseClosed
Posted

Presolicitation

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → Naval Medical Logistics Command
Contacts2 people available
OfficeFORT DETRICK, MD, 21702-9203, USA
Office AddressFORT DETRICK, MD, 21702-9203, USA
Contacts
Burzie C Baker IIIContracting Officer

Full Description

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The Naval Medical Logistics Command intends to negotiate on a sole source basis (IAW FAR 13.501) with ScriptPro USA, Inc, 5828 Reeds Rd, Shawnee Mission, KS 66202, as the only responsible source that can provide an expansion to the proprietary ScriptPro robotic medication dispensing system currently installed at the facility. The requirement is for a robotic prescription dispensing system. The robotic prescription dispensing system shall be able to automatically select a prescription vial of the proper size, fill the vial with the proper medication and print and apply the correct prescription label. The system shall use bar codes to confirm correct drug product and strength. Vials shall be filled directly from drug dispensing cells to prevent cross-contamination. The vial shall be collated, uncapped for the pharmacist to perform a final verification. The system must be compatible with proprietary ScriptPro products. The electrical requirement for the systems is 120 VAC, 60 Hz, single phase. Regulatory Requirements: The system and all of the components, shall be compliant with the Food and Drug Administration (FDA) requirements to market and deliver medical products for use in the United States of America, even should delivery be requested outside of the United States. The claims made for the product shall comply with the regulations of the FDA with respect to products for marketing and delivery of a medical product for use in the United States of America, even should delivery be requested outside of the United States. This acquisition is being conducted under simplified acquisition procedures FAR 13.501 under the authority of the test program for commercial items (section 4202 of the Clinger-Cohen Act of 1996). There are not set-aside restrictions for this requirement. The intended procurement will be classified under North America Industry Classification System (NAICS) 454390. This notice of intent is not a request for competitive proposals and no solicitation document exists for this requirement. However, parties interested in responding to this notice will need to submit technical data, including cost, sufficient to determine capability in providing the same product. All capability statements received by the closing date of this synopsis will be considered by the Government. A determination by the Government not to compete based on responses to this notice is solely within the discretion of the Government. Information received will be considered solely for the purpose of determining whether to conduct a competitive procurement. Capability statements shall be submitted by email only as a MS Word or Adobe PDF attachment to erin.cotter@med.navy.mil. No phone calls accepted.

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