Monday, November 25, 2024

FDA RFI: ORA Quality Management Information System (QMiS)

Solicitation FDA-RFI-FY20-QMIS

The Food and Drug Administration (FDA), Office of Regulatory Affairs (ORA) requires a commercial product, to automate its quality management procedures and centralized document management.

The FDA has a COTS software requirement to provide business analytics solution for wide array of business domains. The contractor’s software shall be compliant with the following salient characteristics:

MasterControl Server or Equal Software

Compatibility with existing FDA environment: The software shall be compatible to support FDA’s existing analytics environment and provide seamless integration with all the existing systems that utilize this environment.

Enterprise scalability: The software shall be highly scalable to support enterprise level users and support growth.  Provide capabilities to serve mobile clients, web clients and desktop-installed software.

Support High Availability: The software shall provide high availability with automatic failover capabilities.  The software shall also send automated email alerts in case of a failover to specified administrators.

Ease of use: The software shall provide an ability to create and modify web-based interactive dashboard and visualization without requiring extensive training on the software.  The software shall be compatible with various web browsers, including Internet Explorer, Firefox and Google Chrome…

Read more here.

Note: G2X has noticed that Beta.Sam has been experiencing some issues during this initial stage of release. We have done our best to ensure links we are sharing here are correct but please understand that you may experience issues with the site.

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Jackie Gilbert
Jackie Gilbert
Jackie Gilbert is a Content Analyst for FedHealthIT and Author of 'Anything but COVID-19' on the Daily Take Newsletter for G2Xchange Health and FedCiv.

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