This Sources Sought opportunity from Department Of Health And Human Services was posted on March 12, 2024. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

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Request for Information: Next-Generation Imports Screening Decision Support Risk Targeting System

Closed

FDA-RFI-75F40124Q00178Federal

Submission Closed03/28/2024, 04:00:00 PM UTC

Contract Overview

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

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NAICS: 541512

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SLED

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Hattiesburg Clinic operates two high-availability (HA) pairs of next-generation firewall (NGFW) appliances one HA pair at the Support Services campus and one HA pair at the Orthopaedics campus, where the Clinic's secondary Internet circuit terminates

Solicitation # 4618-20260930092701

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Solicitation # ocds-h6vhtk-0789d8

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Puc300000 Administration Puc4

POSTED

1 day ago

DEADLINE

in 13 days

General Info

Agency

Department Of Health And Human Services → FDA Office Of Acq Grant Svcs

NAICS

541512 - Computer Systems Design Services

Place of Performance

Silver Spring, MD, USA

Set-Aside

SBA

Documents

FDA RFI: Next-Generation Imports Screening Decision Support Risk Targeting System

rfi

High

AI Contract Breakdown

Uniform Contract Format

Contract not broken down yet

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Timeline

PhaseClosed

PostedMar 12

Sources Sought

Response DeadlineMar 28

Deadline has passed

Submission Closed

03/28/2024, 04:00:00 PM UTC

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Organization & Contact Information

AgencyDepartment Of Health And Human Services → FDA Office Of Acq Grant Svcs

Contacts1 person available

OfficeBeltsville, MD, 20705, USA

Organization / AgencyDepartment Of Health And Human Services → FDA Office Of Acq Grant Svcs

Office AddressBeltsville, MD, 20705, USA

Contacts

Noah Padilla

contact@example.gov

Full Description

FDA's Import Program is responsible for ensuring that all imported products comply with FDA regulations. If FDA determines through examination, sampling, or otherwise that a product is adulterated or misbranded, the product is subject to refusal of admission into the United States in accordance with Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act. FDA receives large quantities of product and product-associated information, and, upon receipt in the form of import entries, a best course of action needs to be decided to protect public health. Legacy systems handling these data are generally siloed and limited, with the creation of interfaces or expansions being time-consuming. Given advancing technologies, it is sought to transition to more flexible decision support systems for screening these entries that are capable of handling large amounts of data while supporting the general operational processes already in place.