Supra
LEGAL · ENGINEERING SAFETY

Safety & Acceptable Use

Version 1.0 · Effective August 21, 2026

Supra assists; humans authorize. Never manufacture, energize, implant, fly, drive, lift, pressurize, medicate, or expose a person/environment based only on Supra output. A green software check is not proof of safety or compliance.

1. Mandatory engineering controls

For every consequential design, you must define requirements and operating envelopes; identify assumptions and unknowns; verify units and coordinate frames; use authoritative material/component data; independently review geometry, tolerances, joints, loads, failure modes, electronics, controls, firmware, cybersecurity, and manufacturing; run appropriate analytical and high-fidelity analyses with convergence and uncertainty evidence; prototype and physically test under foreseeable normal, fault, misuse, and environmental conditions; preserve traceability; resolve every hard-gate failure; and obtain approval from competent, authorized humans.

Images, simulations, surrogates, AI judgments, and plausibility are not substitutes for calibrated measurement. Provider “common sense” is not spatial or engineering evidence. If output conflicts with a deterministic check, standard, drawing, datasheet, test, or qualified reviewer, treat it as failed until resolved.

2. Prohibited uses

3. High-consequence and regulated domains

The free beta is not approved as the sole or controlling system for aerospace/spaceflight; autonomous or road vehicles; rail or marine safety; medical devices, diagnosis, implants, prostheses, life support, or human research; nuclear/radiological systems; power grids and critical infrastructure; pressure vessels and process plants; cranes, hoists, elevators, guards, and industrial machinery; firearms, ammunition, energetics, or military targeting; buildings/structural systems; cleanroom/semiconductor safety; or environmental-control systems.

Use in such domains requires a separate written authorization from Silvia AI where offered, plus all applicable licensed professionals, quality systems, standards, hazard analyses, independent verification and validation, cybersecurity review, controlled configuration, regulator/notified-body interaction, and physical qualification. The user remains the legal manufacturer/deployer and release authority unless a signed agreement expressly says otherwise.

4. AI-specific risk controls

5. Manufacturing and physical experiments

Before fabrication, review material/process compatibility, dimensions and tolerance stack, tooling, workholding, machine envelope, collision, feeds/speeds, support removal, heat treatment, surface finish, inspection plan, PPE, ventilation, fire/chemical hazards, and applicable code. Simulate toolpaths using the machine’s authoritative system. A human operator controls machine start.

Automated experiments require a signed safety envelope, physical interlocks, e-stop, bounded energy/material/temperature/pressure/speed, calibrated sensors, preconditions, abort criteria, supervision appropriate to risk, post-test inspection, and incident logging. The AI must never modify or bypass the governor.

6. Electrical, firmware, and mechatronics

Verify mains isolation, protective earth, fusing, creepage/clearance, insulation, enclosure/fire rating, voltage/current/power/thermal budgets, battery protections, connector pinout and accessibility, grounding/EMC, fail-safe states, watchdogs, update/recovery paths, and applicable ERC/DRC. Compile and test firmware on the exact target. Unexpected ERC/DRC, invalid voltage/pin assignment, firmware failure, or mechanical collision blocks release.

7. Medical, biometric, and personal data

Supra has no general HIPAA BAA, regulated medical-device quality certification, or clinical authorization. Do not use it for diagnosis, treatment, patient-specific manufacture, implant release, or clinical decisions. De-identification must be performed before ingestion and independently assessed. Human-subject and biometric work requires ethics, consent, privacy, security, and regulatory review.

8. Export, security, and dual-use review

Classify controlled software/technology and screen destination, end user, ownership, end use, and deemed-export access. Do not assume a public download makes an end use lawful. Follow applicable EAR, ITAR where relevant, OFAC sanctions, EU/UK and other controls, organization policies, and license conditions. Report suspected diversion or compromise to appropriate compliance personnel.

9. Reporting and enforcement

Stop use when Supra behaves dangerously, evidence is inconsistent, calibration is stale, provenance is missing, or a hard gate fails. Preserve the project, version, logs, inputs, outputs, and evidence without exposing secrets; contact hello@silviaai.dev. Silvia AI may restrict features or terminate access for credible dangerous or unlawful use. Emergency situations must be handled by local emergency services and qualified personnel, not product support.

10. Regulatory responsibility

Supra may fall within different AI, product, professional, consumer, privacy, cybersecurity, employment, sector, and machinery regimes depending on deployment. You must classify your use. If you deploy Supra as a component of a high-risk system, substantially modify it, or place an AI-enabled product on the market, you may acquire provider, deployer, importer, distributor, or manufacturer duties. These policies do not perform that assessment or transfer those duties.