This Sources Sought opportunity from Department Of Health And Human Services was posted on November 14, 2024. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

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PrecisionFDA Request for Information

Closed

75F40125Q00036Federal

Submission Closed11/15/2024, 05:00:00 PM UTC

Contract Overview

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

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NAICS: 518210

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POSTED

DEADLINE

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POSTED

DEADLINE

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NASA Shared Services Center

POSTED

1 day ago

DEADLINE

in 1 day

General Info

Agency

Department Of Health And Human Services → FDA Office Of Acquisitions And Grants Services

NAICS

518210 - Computing Infrastructure Providers, Data Processing, Web Hosting, and Related Services

Place of Performance

Silver Spring, MD, USA

Set-Aside

NONE

Documents

PrecisionFDA Request for Information (RFI)

rfi

Low

AI Contract Breakdown

Uniform Contract Format

Contract not broken down yet

CLEATUS splits the solicitation into Uniform Contract Format (UCF) sections: scope, pricing, deliverables, and evaluation criteria.

Timeline

2 updates

PhaseClosed

PostedNov 7

Sources Sought

Notice updatedNov 8

Notice details unchanged. Attachments may have changed.

Deadline changedNov 14

Response deadline changed from Nov 14, 2022 to Nov 15, 2024.

Response DeadlineNov 15

Deadline has passed

Submission Closed

11/15/2024, 05:00:00 PM UTC

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Organization & Contact Information

AgencyDepartment Of Health And Human Services → FDA Office Of Acquisitions And Grants Services

Contacts1 person available

OfficeRockville, MD, 20857, USA

Organization / AgencyDepartment Of Health And Human Services → FDA Office Of Acquisitions And Grants Services

Office AddressRockville, MD, 20857, USA

Contacts

Jada Scott

contact@example.gov

Full Description

The Food and Drug Administration (FDA) plays an integral role in precision medicine initiatives, which foresees the day when an individual's medical care will be tailored in part based on their unique characteristics and genetic make-up. To this end, the FDA is developing the tools, standards, and approaches needed to ensure that genomic tests provide reliable and accurate genetic results. This effort is one part of the FDA's commitment to leverage external resources and expertise to advance regulatory science, the science that is essential for product development and evaluation and which underpins the FDA's regulatory decision-making. PrecisionFDA is a FISMA-authorized secure cloud-based portal, analysis platform and data repository which enables collaboration and sharing of large datasets by reviewers, bioinformaticians, researchers, and data scientists from industry, academia, government, and other partners. Specifically, precisionFDA enables collaboration between FDA researchers and reviewers, as well as external collaborators and sponsors to come together to foster and develop the regulatory science to support regulation of multi-omics and Real-World Data (RWD) informatics in drugs and devices. This includes genomics, transcriptomics, proteomics, metabolomics, imaging, and electronic health record data from healthcare partners. This integration of multi-omics and RWD is helping to deliver safe and effective treatments precision-tailored to individuals and groups, thus the name precisionFDA. This contract includes the maintenance of the current operational system, as well as enhancements to that system. The diagram below visually conveys the current scope and uses of the precisionFDA program.