Healthcare & Pharma
USP-grade water. Legionella-free systems. Full USFDA audit trails.
Healthcare facilities and pharmaceutical manufacturers require water purity standards that far exceed industrial norms — and the documentation trail to prove it at every regulatory audit.
Industry Challenges
What makes healthcare & pharma water treatment complex.
Every industry has unique water treatment requirements. Understanding these sector-specific challenges is the starting point for every NWPL project.
USP Purified Water (PW) and Water for Injection (WFI) require conductivity <1 µS/cm and TOC <100 ppb — municipal supply cannot meet this without advanced treatment.
Cooling tower water in hospitals creates Legionella risk that has caused fatalities. ASHRAE 188 compliance requires active biocide management and regular monitoring.
USFDA and WHO-GMP audits demand complete documentation: DQ, IQ, OQ, PQ reports, ongoing deviation logs, and calibration certificates for all monitoring instruments.
Pharmaceutical effluent contains APIs (Active Pharmaceutical Ingredients) and solvents that require specialised biological and chemical treatment — standard ETP processes are inadequate.
Central Sterile Supply Departments (CSSDs) need water purity certified to European Standard EN 285 for autoclave feed — another separate water quality standard.
Our Solutions for Healthcare & Pharma
Technology matched to your site.
Compliance Requirements
Pharma and healthcare have the most complex water compliance requirements in any industry.
NWPL systems are designed to meet every applicable standard for your sector — from the day of commissioning.
USP 40 <1231>
Water for Pharmaceutical Purposes — PW, WFI, and Purified Water specifications
USFDA 21 CFR Part 211
Current Good Manufacturing Practice — water system validation requirements
WHO-GMP TRS 929
WHO Good Manufacturing Practices — pharmaceutical water quality
ASHRAE 188-2018
Legionella risk management programme for cooling water systems
EN 285
European Standard for steam sterilisation — feed water quality for autoclaves
CPCB / MPCB / GPCB
State PCB consent for pharmaceutical effluent discharge (API limits)
Featured Projects
Proven in healthcare & pharma.
USP Purified Water System — 50 KLD, Hyderabad
Double-pass RO + EDI delivering 0.06 µS/cm conductivity. Three years of operation with zero OOS incidents. System validated to USFDA 21 CFR requirements with complete IQ/OQ/PQ documentation.
Pharmaceutical ETP — 250 KLD, Pune
COD consistently ≤200 mg/L. API removal >99.5% verified by NABL-accredited lab. MPCB consent maintained. Zero show-cause notices in 2 years.
Get a Pharma-Specific Proposal
Every site is different. Every system NWPL designs is different. Tell us your constraints — we'll handle the engineering.