We are seeking qualified contractor or individual developer to submit proposals for the development of a single-user Unity-based Mixed Reality (MR) prototype targeting the PICO 4 Ultra Enterprise device. The prototype will deliver a hands-free, gaze-controlled, and voice-activated interface to guide users through procedural process-flows using checklists stored in external YAML files.
This solution is designed as an early demonstration application to showcase immersive productivity and training capabilities within enterprise and industrial workflows.
The objective of this contract is to work with us to design, co-develop, and deliver a working Mixed Reality prototype application on the PICO 4 Enterprise using Unity, that includes the following:
Protocol Title: "Sterile Compounding Room Startup"
Protocol Title Description: "Validated protocol for initiating sterile manufacturing operations in Grade A/B Cleanroom."
Protocol Introduction: >
This protocol outlines the validated steps required to initiate operations in a sterile production suite.
All steps must be completed in sequence and signed off digitally or via voice/gaze control.
Protocol PreRequisites: >
Ensure personnel are properly gowned according to SOP-001-A.
Confirm environmental monitoring system is operational.
Confirm HVAC and HEPA filtration systems have been running continuously for a minimum of 30 minutes prior to start.
Protocol Safety Instructions: >
All operators must adhere strictly to aseptic techniques.
No unauthorized materials may enter the Grade A zone.
Report any anomalies to the QA Supervisor immediately.
Protocol Primary Contact: "Dr. Lisa Meinhart, QA Supervisor, Ext. 2205"
Protocol Steps:
- step: 1
title: "Enter Gowning Room"
instructions: "Follow full-body sterile gowning procedure according to SOP-001-A. Use mirror to verify full coverage."
- step: 2
title: "Perform Initial Cleanroom Disinfection"
instructions: "Using sterile wipes saturated with sporicidal agent, disinfect all high-touch surfaces in the Grade B area."
- step: 3
title: "Activate Cleanroom Monitoring Systems"
instructions: "Check and activate particle counter, differential pressure monitors, and temperature/humidity sensors. Log values."
- step: 4
title: "Prepare and Stage Materials"
instructions: "Transfer pre-approved sterile materials into the pass-through chamber. Wipe down each item with 70% IPA."
- step: 5
title: "Perform Airflow Smoke Test (Visual Confirmation)"
instructions: "Use sterile smoke wand to visualize unidirectional airflow across work surfaces. Confirm laminar flow integrity."
- step: 6
title: "Verify HEPA Filter Functionality"
instructions: "Check filter status indicators or refer to Building Management System (BMS) for real-time performance data."
- step: 7
title: "Confirm Line Clearance"
instructions: "Verify that the production suite is free from any previous batch remnants, with QA sign-off completed."
- step: 8
title: "Document Environmental Parameters"
instructions: "Log temperature, RH%, differential pressure readings in the batch record or eBR."
- step: 9
title: "Sanitize Gloves and Enter Grade A Zone"
instructions: "Sanitize sterile gloves with 70% IPA spray before entering the aseptic processing area."
- step: 10
title: "Begin Batch Execution"
instructions: "Initiate batch record by scanning lot ID and confirming material and equipment readiness."
We expect a delivery window of 10 days, starting from contract signature.