From GMP-validated production zones to cold-chain warehouses — we deliver third-party WiFi heatmap, RF site surveys and validation reports your QA, compliance and IT teams can stand behind.
Direct engagements. Independent reports. Repeat partnerships.
Additional Fortune 500 and global pharma clients referenced anonymously per confidentiality agreements — see Selected Engagements below.
Pharma facilities have constraints no enterprise vendor accounts for — ATEX zones, stainless-steel reflective surfaces, high-density IoT, and traceability that auditors will question.
HEPA walls, stainless equipment and gowning rooms create RF shadows that standard surveys miss.
A 30-second WiFi drop on a packaging line can mean a full batch hold and CAPA paperwork.
Auditors increasingly ask for independent documentation of network infrastructure performance — not just OEM self-certification. Our reports are structured to fit into your IT qualification (IQ/OQ/PQ) and CSV documentation workflows.
Vaccine warehouses and stability chambers depend on uninterrupted sensor telemetry — 24×7×365.
Some clients referenced anonymously where confidentiality agreements apply.
Predictive RF modelling and on-site Access-Point-on-a-Stick (APoS) validation at Ferring's Mumbai Product Development Centre, followed by post-implementation validation against design intent. Sign-off documentation aligned to the client's IT validation SOPs.
Predictive coverage modelling for sterile injectables manufacturing environment, followed by independent post-implementation validation. Reports structured to support FDA-regulated facility IT documentation.
Access-Point-on-a-Stick validation followed by post-implementation verification across formulations and QC areas. Independent verification of installed WiFi against design intent.
On-site APoS validation and post-implementation verification across the formulation manufacturing facility. Coverage and AP placement validated against design intent.
Independent post-implementation validation of installed wireless infrastructure at a leading Indian pharmaceutical major's formulations facility. Acceptance reporting and URS compliance documentation.
From sterile cores to ambient warehouses — our engineers come prepped for every environment.
Aseptic filling, weighing booths, gowning rooms
HPLC, instrumentation, stability rooms, micro labs
Vaccine storage, raw material vaults, finished goods
Tablet compression, blister lines, serialization
Floor-by-floor signal, SNR, channel & roaming visualization across production blocks, QC labs and warehouses — using calibrated Ekahau Sidekick devices.
Designing a new plant or expansion block? Our predictive modelling and on-site Access-Point-on-a-Stick validation guarantees coverage before AP procurement.
Independent verification that your installed WiFi meets the design intent — with sign-off documentation aligned to your IT-validation SOPs.
Persistent disconnects on the packaging line? Slow handheld scanners in stores? We diagnose root cause and deliver a corrective action plan.
Every engagement ends with a structured deliverable engineered for both IT decision-making and audit defense.
30-min consultation on your facility, applications & compliance needs.
Certified engineer arrives with calibrated Ekahau & NetAlly tools.
Heatmaps, gap analysis & remediation plan delivered in 5 working days.
Executive readout with your IT, QA & validation stakeholders.
We don't sell access points. We don't push hardware. That independence is why pharma IT and validation teams use our reports as supporting documentation in infrastructure qualification — referenced during internal audits and regulatory inspections, including USFDA, WHO-GMP and EU-GMP frameworks.
Kloudwifi provides independent wireless infrastructure assessment services. Our reports are designed to support customer IT qualification and validation processes. Final compliance determination rests with the customer's QA, validation and regulatory affairs teams.
Working with Kloudwifi gave our IT and validation teams a single, vendor-neutral source of truth on wireless coverage across our Manufacturing and Warehouse. The heatmaps, gap analysis and remediation plan were detailed enough to feed directly into our infrastructure-qualification documentation — and the engineers understood what a cleanroom audit-trail actually requires.
Kloudwifi's post-implementation validation gave our IT and QA teams the independent verification we needed before sign-off. The walkthrough session and remediation plan were exactly what our infrastructure qualification process required.
Talk to a pharma WiFi specialist today. Get a no-obligation scoping call and indicative quote within 24 hours.