Two buyer profiles, one engineering posture.
Sense7ai builds web applications for enterprise teams under a regulatory frame and for production-grade builders outside formal regulation. The Core Web Vitals targets, accessibility commitments, observability instrumentation, and exit provisions are the same for both — only the specific compliance overlay changes.
Teams in financial services, healthcare, pharma, or other regulated operating frames — web applications engineered to GLBA, HIPAA, FDA, or sector-equivalent requirements. Accessibility, audit-grade approval surfaces, and reviewer-facing control interfaces scoped from day one.
Teams outside formal regulation who want the same engineering posture — Core Web Vitals budgeted at sprint zero, WCAG 2.2 AA built in from day one, structured observability instrumented from sprint one. New builds, codebase upgrades, or capability extensions.
Throwaway landing pages · brochure microsites with no operational surface · single-page client work that will not outlive a campaign · projects that need a body shop rather than an engineering team.
Customer-facing, internal, and B2B web platforms.
Sense7ai's web application practice covers customer-facing platforms, internal operational tooling, and B2B portals. Where applications handle consequential actions — approvals, access decisions, regulated data submissions — human-authorisation steps are defined at the design stage, not added as an afterthought.
For regulated enterprises running AI-assisted workflows, the web application layer is the human-control surface — the interface where reviewers examine AI outputs, exercise their approval authority, and generate the audit record that satisfies a regulator.
Customer-facing web platforms.
Multi-tenant SaaS platforms, self-service portals, and application interfaces designed to perform across device types and network conditions. Real User Monitoring is instrumented from sprint one; performance targets are set before build begins.
- Zitarecruiter-facing applicant tracking interface
- ArkOSclient-facing CRM and lifecycle management modules
- Verixareviewer-facing pharma audit and deviation interface
Five phases. Performance and accessibility budgeted.
What we work with.
Frontend: React (Next.js, Remix), Vue (Nuxt), Svelte / SvelteKit, vanilla TypeScript. Component systems: Radix, Headless UI, custom design systems built with Storybook. Styling: CSS modules, Tailwind, vanilla-extract. State and data fetching: Zustand, Jotai, Redux Toolkit, TanStack Query. Testing: Vitest, Playwright, Cypress. Performance: Lighthouse CI, WebPageTest, Chrome User Experience Report integration. Accessibility: axe, Pa11y, manual screen-reader testing (NVDA, JAWS, VoiceOver, TalkBack). Microsoft Power Platform: Power Apps, Power Automate, Power BI; Microsoft 365 ecosystem integration (SharePoint, Teams).
We work in your environment. The specific frameworks and tools for any engagement are agreed during discovery, reflecting your existing stack, team preferences, and integration constraints. The list above is the range our engineering team works in.
Shipped engagements.
Current production engagements include Aeonn Ark Group portfolio companies (Zita, ArkOS) and an independent client (Verixa) — affiliation disclosed in diligence, see security.
ArkOS
Multi-module enterprise web platform
Web application layer across six business modules — CRM, Sales & Marketing, Client Lifecycle Management, Operations, Finance, and Compliance. Role-based access controls with human-authorisation on every consequential operation.
Read case study →● In productionZita
Recruiter-facing applicant tracking interface
Application interface for recruiters to review AI-assisted candidate rankings, manage pipelines, and schedule interviews. Designed so the recruiter remains the decision-maker; AI recommendations are surfaced with explanations, not presented as verdicts.
Read case study →● In productionVerixa
Reviewer-facing pharma audit interface
Audit trail and deviation-tracking interface for pharma-regulated operations. Reviewers examine records, exercise approval authority, and generate the evidence trail that satisfies 21 CFR Part 11 inspection requirements.
Read case study →