RFI_Form.docx

U.S. Food and Drug Administration Request for Information Form

Physical Access Control System Request for Information No: FDA-RFI-1150599

Company Overview

Name of PACS solution provider

Name of contact person

Title

Telephone number

Email address

Mailing address

Company website address

Company’s primary line of business

Product information

Please describe your PACS solution, including specific functionality and features.

What difficulties have you encountered when implementing your PACS, and what were your lessons learned?

Does your PACS solution provide for a licensed, integrated, nationwide solution?

Specific product functionality

Can your PACS solution support Sensitive Compartmented Information Facilities (SCIFs)?

Please provide the capabilities of your PACS’ visitor management system.

The FDA’s IT architecture includes the following infrastructure software stacks (see below). Can your PACS operate under this type of IT architecture? If not, why not?

Does your PACS solution have an existing API with Quantum Secure?

Can your PACS solution support the application and database on separate servers?

Timeline

In implementation of your PACS solution on a similar scale, footprint, and complexity to the FDA, what was the general sequence (e.g., pilots, rollout sequencing) across facilities, and how much time/LOE was allocated for each?

What is the general estimated timeframe (e.g., within 6 weeks, within 3 months) by which key product hardware (e.g., panels, readers) would be available for implementation at the scale required for a federal agency with the size, footprint, and complexity of the FDA?

Implementation model

What would be your anticipated labor categories, labor category description/qualifications and Level of Effort for the described need?

Vendor Support

What would be your anticipated labor categories, labor category description/qualifications and Level of Effort for post implementation support/maintenance of the system, to include hardware and software?

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