ROVQIX works remotely with Philadelphia organisations across pharmaceuticals, higher education, health systems and regional B2B, with Eastern-morning overlap. These buyers share two requirements: WCAG 2.2 AA accessibility for procurement, and documented handling of regulated data.
Philadelphia enquiries almost always arrive with a compliance attachment — a university procurement checklist, a pharma security questionnaire, or a health system's data policy. That is the work, not an afterthought.
We're online
Procurement standard
Data flows and controls
USD invoicing
WCAG 2.2 AA with real keyboard and screen reader testing, plus the conformance documentation buyers request.
Access control at the data layer, audit logging and defined retention — the questions pharma and health buyers ask.
Large site architectures with genuine information hierarchy, search and multi-department publishing.
Publication libraries, trial information and technical documentation structured to be findable.
Structured review rounds with deadlines, because committee sign-off is what actually delays these projects.
Completed in writing, with named least-privilege access and revocable credentials throughout.
| Sector | Typical project |
|---|---|
| Pharmaceutical and life sciences | Product and trial information sites, portals |
| Higher education | Department sites, enrolment flows, accessible content |
| Health systems | Patient portals and provider directories |
| Professional services | Credibility sites for long sales cycles |
| Regional manufacturing | Distributor portals and specification libraries |
Because approval is distributed across departments, and nobody owns the decision until it is named upfront.
We build the technical controls — access control, audit logging, encryption, minimal data exposure, documented data flows — and we complete vendor security questionnaires. Policy, workforce training, formal certification and legal determination sit with you and your compliance advisors.
We will map that boundary explicitly in the proposal rather than implying we deliver compliance as a whole. Any vendor claiming otherwise from a website build is overstating what software alone can do.
No. We are a remote studio based in India working with Philadelphia clients, with Eastern-morning overlap and US-standard contracts. We will not list a virtual address to suggest otherwise.
We build to WCAG 2.2 AA and provide detailed conformance documentation. For a formally signed VPAT, an independent accessibility firm is the correct route and we remediate against their findings.
Yes. We complete vendor questionnaires in writing, work under named least-privilege accounts, never copy production data to development, and support background verification.
Typically 50 to 100% longer than an equivalent commercial project, almost entirely due to review and procurement cycles. We build that into the schedule rather than discovering it later.
How we think about this work, in more depth.
Philadelphia
A 30-minute call, then a written proposal with scope, price and timeline within two to three working days. No retainer required to get a real number, and no obligation if the answer is that we are not the right fit.