Purified water engineered for regulated environments.
SaniSpec brings sanitary, cGMP-aligned design to USP Purified Water applications in pharmaceutical, biotech and related facilities. Configure RO/DI treatment, microbial control and monitoring around your water-quality requirements and qualification scope.
Built around your water-quality requirements.
Regulated applications call for more than a laboratory water rating. SaniSpec brings treatment, sanitary operation and documentation into the same design conversation.
Water quality beyond a single reading
Define USP Purified Water requirements alongside the intended use. Conductivity, organic content and microbial control need to be considered together; a resistivity target alone does not define the complete requirement.
Sanitary operation throughout the system
Hygienic flow paths, drainability and sanitary connection options support the operating strategy. Materials, sanitization and distribution are selected together for your application.
Qualification planned with the equipment
Agree the monitoring, records and documentation needed by the site before the system is built. Qualification activities and acceptance criteria remain part of the project’s defined scope.
Inside the SaniSpec system.
The treatment train and distribution arrangement follow your application. Review the complete water path rather than selecting each stage in isolation.
RO and DI treatment
Reverse osmosis and DI polishing form the configurable treatment train. Additional upstream or downstream steps follow the feedwater and user requirement specification.
Sanitization and microbial control
Select hot-water or ozone sanitization around the materials and available utilities. UV and sub-micron filtration are available where the microbial control plan requires them.
Storage and recirculating distribution
Coordinate storage requirements and a recirculating loop with demand and points of use. Confirm the storage arrangement, distribution scope and service access during project design.
Final treatment and instrumentation
Point-of-use final filters and optional Type I polishing support specific use requirements. Instrument locations, controls and alarms are defined with the treatment and distribution scope.
Monitoring for operation.
Documentation for qualification.
Specify the instruments, alarms, records and qualification deliverables together. The control package should support day-to-day operation and the site’s agreed review requirements.
Core monitoring and alarms
Conductivity/resistivity and temperature monitoring are standard. PLC/HMI controls provide operator visibility and alarm logging; confirm the project’s alarm points and operating sequence.
Optional instrumentation and integration
A TOC analyzer and BMS/SCADA integration are available options. Define the required signals, remote visibility and data-handling scope with your facility team.
Agreed qualification deliverables
Turnover documentation, IQ/OQ support and available FAT/SAT services can support qualification planning. Confirm deliverables and responsibilities in the project scope; they do not establish automatic regulatory compliance or completed validation.
SaniSpec technical specifications.
Typical published characteristics provide a starting point. Final performance, materials, utilities and documentation follow the selected configuration and project requirements.
Performance & water quality
- Typical production
- 1–10 GPM (3.8–38 L/min); subject to project requirements
- Product water
- USP Purified Water; ASTM Type II
- Point-of-use quality
- Optional Type I polishing
Treatment & sanitization
- Primary treatment
- Reverse osmosis with configurable DI polishing
- Sanitization options
- Hot water or ozone
- Additional microbial control
- UV and sub-micron filtration options
Distribution & materials
- Distribution
- Recirculating loop support; point-of-use final filters
- Materials & finishes
- Hygienic, sanitary construction; selected to the user requirement specification (URS) and site standards
- Utilities
- Electrical, feedwater and drain sized to selected flow; heat load depends on sanitization mode
Monitoring & controls
- Standard monitoring
- Conductivity/resistivity and temperature
- Optional instrumentation
- TOC analyzer
- Controls
- PLC/HMI with alarm logging
- Facility integration
- BMS/SCADA integration options; scope defined for the project
Documentation & qualification
- Turnover
- Turnover documentation package
- Qualification support
- IQ/OQ support; FAT/SAT available by agreed scope
USP Purified Water is the intended application. The site must establish its water-quality requirements, qualification plan and acceptance criteria; no blanket certification or compliance guarantee is implied.
Bring the requirements. Review the whole installation.
Share your defined water requirements, URS or equipment schedule. PPT can review treatment, utilities, distribution and documentation together, including what the team needs to operate and service the system.
Useful information to share
- Required water quality and intended applications
- Daily use, peak demand and feedwater characteristics
- Storage, distribution and points of use
- Sanitization requirements and available utilities
- Monitoring, controls and documentation expectations
- Facility layout, access and service clearances
Questions before the next step.
Clarify project scope before committing to a configuration.
Does selecting SaniSpec complete system validation?
No. A sanitary, cGMP-aligned design does not establish certification or completed validation. Site requirements, the selected configuration, qualification activities and acceptance criteria must be agreed and assessed for the project.
What if our demand is above the typical range?
Discuss daily and peak demand, storage and distribution with PPT. SkidSpec or a custom engineered approach may provide a more appropriate starting point for requirements above the typical SaniSpec range.
Review SkidSpecWhat affects the project schedule?
Instrumentation choices, sanitization mode, material requirements and the documentation scope influence lead time. Confirm these decisions and the required review milestones with PPT early in planning.
Review your sanitary water specification with PPT.
Share your water-quality criteria, use points, sanitization requirements and documentation scope. PPT can review SaniSpec treatment, monitoring and distribution with your engineering and quality teams.