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This Combined Synopsis/Solicitation opportunity from Department Of Health And Human Services was posted on September 1, 2020. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Professional Support Services to Enhance Genetic and Rare Disease Content on MedlinePlus.gov

Closed
75N97020Q00031MSFederal

Contract Overview

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

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General Info

NAICS

519130 - Internet Publishing and Broadcasting and Web Search Portals

Place of Performance

MD, USA

Set-Aside

NONE

Documents

9

Amendment+1.pdf

PDF

Attachment+1_SOW75N97020Q00031MS.pdf

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Attachment+2a+52_212_4-OCT+2018_508.pdf

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Attachment+2b+52.212-5_20190809.pdf

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Attachment+3_Invoice+Submission+via+Email+to+NIH+OFM.pdf

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Attachment+4_Information+And+Physical+Access+Security+Statements.pdf

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Attachment+5_52.204-24_20190809.pdf

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Attachment+6_52.204-25_20190809.pdf

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RFQ+75N97020Q00031MS.pdf

PDF

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Timeline

1 update
PhaseClosed
Posted

Combined Synopsis

Deadline changed

Response deadline changed from Sep 1, 2020 to Sep 3, 2020.

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → National Institutes Of Health Nlm
Contacts2 people available
OfficeBETHESDA, MD, 20892, USA

Full Description

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The purpose of this contract is to maintain MedlinePlus by ensuring its genetic and rare disease content is updated and enhance the information by providing a patient's perspective. Incorporation of the patients' perspective in health information is critical to ensure that content created reflects topics, which matter most to patients, and encourages patient participation in decision-making and self-management. Tangible deliverables of this contract consist of "Alerts" for updates to existing materials as detailed in Section D (Tasks to be Performed), below. The - Alerts, will highlight content that needs to be updated (for example, a new gene associated with a particular health condition) or confirm that the existing content is accurate and does not need any changes. This project will leverage the skills and resources of an organization with access to a broad variety of genetic and rare disease support and advocacy groups. The contractor will use their contacts among the various genetic support and advocacy groups. The services will build on existing processes, templates, and documentation established and refined over the past 9 years to update Genetics Home Reference content which is being transitioned to MedlinePlus.

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Miguel
Hillary
Keith Deutsch
Christine

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