Justification
Limited Sources Justification for CBER OM Operations and Systems Support
47QTCA18D005G_75F40124F80303
Food and Drug Administration, FDA Office of Acq Grant SVCS. Other Computer Related Services.
Status
Justification
Posted September 2, 2024. Scheduled to archive October 2, 2024.
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Description
As published on SAM.gov.
The purpose of this acquisition is to award a follow-on task order to Guidehouse Inc. in support of the Center of Biologics Evaluation and Research (CBER), Office of Management (OM); to be issued under GSA Multiple Award Schedule (MAS) contract number 47QTCA18D005G. The follow-on order is to provide services to support CBER OM’s highest priority workforce management systems; the Biologics Planning and Execution Reporting System (BPERS) and PathHR applications.
These two key applications, which manage CBER’s financial, acquisition, travel and human resources, require continuous system development, modernization and enhancements (DME) as well was operations and maintenance (O&M).
As part of the evolution of CBER’s administrative functions, OM requires support for business processes and operational support to improve, refine, and enhance operations for the payroll, travel, and the Inter Agency Agreement (IAA) and Oak Ridge Institute for Science and Education (ORISE) programs. The purpose of this project is to procure contractor support services to assist OM/DABR in: PathHR system enhancements to support current and future FDA and Center-level HR initiatives.
BPERS operations and analysis support to assist end users utilize the application and manage budget planning and execution activities effectively. Business process improvement and operational support for the Travel Team and CBER’s Inter Agency Agreement (IAA) and Oak Ridge Institute for Science and Education (ORISE) programs
Publications
Every notice SAM.gov issued under this solicitation number, oldest first. Each is a separate record on SAM.
September 2, 2024
Justification
SAM.gov, notice 68eec057a00b4873a793eeedfef0f59a
Points of contact
- Michelle Dacanaymichelle.dacanay@fda.hhs.gov