Your Purest Input Deserves
a Cleaner Origin.

Ultra-pure water for pharma — no groundwater, no RO waste.

Get the Tech Dossier →How it works

Every litre of RO-purified water
wastes three more.

Pharmaceutical manufacturing demands ultra-pure water — and today, that means reverse osmosis systems that reject 60–75% of the water they process, draining borewells faster than monsoons can refill them.

Water stress is already disrupting production schedules in Chennai, Hyderabad, and Pune. The next decade will make it a supply-chain risk every pharma operator must price in.

Water wasted for every litre purified by conventional RO
40%
Of India's pharma clusters are in water-stressed zones
0
Groundwater drawn by FromAir® — ever

Introducing Uravu's
FromAir® Technology

FromAir® creates water directly from atmospheric humidity — no borewells, no chemicals, no reject stream. The output is mineral-stabilized ultra-pure water that meets pharmacopoeial standards straight from the unit.

  • 100% pure, mineral-stabilized water — no post-treatment required
  • No RO system, no reject water, zero borewell dependency
  • Container-sized, modular units — deploy inside existing pharma parks
  • Validated for injectable lines, R&D labs, and sterile manufacturing
  • Powered by waste heat or low-grade renewable energy
  • GMP-compatible design with full audit trail support
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Atmospheric Source

Uravu's proprietary liquid desiccant absorbs moisture from ambient air — even in low-humidity conditions — creating an inexhaustible, rainfall-independent water source.

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Waste-Heat Regeneration

The desiccant is regenerated using 35–60°C low-grade heat from your existing facility — the same heat your HVAC or process equipment already discards.

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Pharmacopoeial Purity

The condensed water is processed to meet IP/BP/USP standards for Purified Water and Water for Injection, with conductivity, TOC, and microbial compliance built in.

Built for every sterile environment

FromAir® scales from a single R&D bench to a full injectable manufacturing line.

Injectable Lines

WFI-grade output compatible with vial-filling, lyophilisation, and aseptic processing environments.

API Synthesis

Consistent ultra-pure water feed for reaction steps where impurity control is critical to yield.

R&D Laboratories

Right-sized units for pilot batches and analytical work — no infrastructure upgrade needed.

Sterile Formulation

Zero-reject water supply for ophthalmic, parenteral, and topical product lines.

Cleanroom Humidification

Controlled-purity water for HVAC humidification in Grade A/B cleanroom suites.

QC & Validation

Audit-ready water with real-time monitoring for regulatory submissions and internal QA.

What pharma teams are asking

Common questions from regulatory, engineering, and procurement teams.

How does FromAir® meet Water for Injection purity benchmarks?

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Is it validated for cleanroom or GMP environments?

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What redundancy, uptime, and monitoring controls exist?

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Can it deploy inside an existing pharma park or SEZ?

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What happens when ambient humidity is very low?

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Want answers?

Drop your details and we'll send you the full tech dossier — including GMP integration notes, purity data, and indicative costing.

Full FromAir® technical specification
GMP integration & validation notes
Purity benchmark data vs. IP/BP/USP
Indicative CAPEX / OPEX model

Community

Save Water.
Drink Air.

Join the FromAir® Club — a network of pharma teams, sustainability leads, and water-positive advocates building the next era of clean manufacturing.

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