Cleaning Cycles
Cleaning systems for hygienic production lines.
Process Equipment
CIP / SIP Systems for Hygienic Cleaning Workflows.
CIP and SIP systems support cleaning and sterilization workflows for sanitary process lines, tanks and equipment packages.
CIPSIPSkids316L / 304
Applications
Cleaning system support for process operations.
CIP/SIP RFQs should include process layout, utilities, cleaning method and documentation requirements.
Validated Cleaning
High-purity cleaning and sterilization language by RFQ.
Package Systems
CIP/SIP package sourcing for project assemblies.
Sizes & Dimensions
CIP system configurations.
Single-tank, multi-tank or once-through configurations. Pre-engineered packages with chemical dosing, heat exchange, recirculation and PLC control.
| Tank Size | Flow Rate | Heater (kW) | Power (kVA) | Footprint | Application |
|---|---|---|---|---|---|
| 500 L | 5 m³/h | 30 | 40 | 3 × 2 m | Lab / pilot |
| 1000 L | 10 m³/h | 60 | 80 | 4 × 2 m | Small process |
| 2000 L | 20 m³/h | 120 | 150 | 5 × 2.5 m | Medium plant |
| 5000 L | 40 m³/h | 240 | 300 | 6 × 3 m | Large plant |
| 10000 L | 60 m³/h | 360 | 450 | 8 × 4 m | Industrial |
Operating Conditions
Pressure-temperature rating for cip / sip systems.
System operating conditions vary by cycle: caustic at 75-85°C, acid at 50-65°C, SIP at 121-135°C steam.
Service Conditions
- CIP Caustic: 75 – 85°C circulation
- CIP Acid: 50 – 65°C circulation
- SIP Steam: 121 – 135°C
- Rinse: Ambient or 60°C
- Tank pressure: Atmospheric
- Control: PLC + HMI
Actual ratings depend on size, material and operating conditions. Confirm via RFQ for project-specific requirements.
Standards & Compliance
Built to recognized sanitary and pressure standards.
Full documentation packages available including MTR, 3.1 certificates, surface roughness reports and pressure test records.
3-A 78-03
3-A Spray Devices
Sanitary spray cleaning devices standard.
ASME BPE
Bioprocessing Equipment
Surface finish, materials and design for pharma/biotech.
EHEDG
Hygienic Equipment Design
European hygienic engineering and design certification.
ISA-88
Batch Control
Industrial standard for batch process control.
CE / UL
Electrical Safety
Electrical safety certification.
FDA 21 CFR 11
Electronic Records
Electronic records compliance.
Product Variants
CIP/SIP System configurations for different process roles.
Multiple variants available to match your application requirements. Browse related products for complete process line coverage.
Multi-Tank CIP
Multi-tank for simultaneous caustic/acid/rinse with no contamination.
Request quote →Technical Overview
Typical CIP/SIP RFQ fields.
System requirements depend on process layout, utilities, flow, temperature and control expectations.
| Requirement | Typical Information Needed |
|---|---|
| Product Type | CIP / SIP system or package |
| Material Grade | 304 / 316L stainless steel by project |
| Capacity | Flow, temperature, tank capacity and cleaning cycle |
| Integration | Process connections, utilities and controls |
| Documentation | Drawings, P&ID, BOM and certificates |
Engineering RFQ
Prepare a CIP/SIP RFQ.
Include system type, process application, flow/capacity, utilities, drawings and documentation needs.
- Size / connection / material grade
- Quantity and target lead time
- Drawing, BOM or existing part reference
- Documentation and finish requirements
Documentation by RFQ
Material certificates, finish notes, inspection requirements, heat traceability and supplier documentation can be included in the quotation package.
Have a CIP/SIP requirement?
Send process layout, system type, capacity, drawings and documentation requirements.
Engineering Documentation
Technical Datasheet Available
Download the product datasheet for technical specifications, dimensional references, material data, applicable standards and RFQ guidance. Suitable for procurement, engineering review and project documentation.
Common Questions
Frequently asked questions about cip / sip systems.
Engineering and procurement questions we hear most often. For project-specific guidance, send your application details via RFQ.
What is the difference between CIP and SIP?
CIP (Clean-in-Place) uses chemical cleaning at 50-85°C. SIP (Sterilize-in-Place) uses pressurized steam at 121-135°C for sterilization.
CIP removes soil and disinfects; SIP achieves sterilization (>6 log reduction). Pharma/biotech typically require both.
How do I size a CIP system?
Flow rate per circuit: 3-5 m³/h per square meter of tank surface, or 1.5-2 m/s velocity in piping. Tank volume: 1.5-2× single circuit volume.
Provide largest tank dimensions, piping diameters, number of circuits, simultaneous use. Energy/utility load also calculated from cycle frequency.
What is a typical CIP recipe?
Standard: 1) Pre-rinse (water, 5-10 min), 2) Caustic wash (1-2% NaOH, 70-85°C, 15-30 min), 3) Intermediate rinse, 4) Acid wash (1-2% HNO3, 50-65°C, 10-15 min), 5) Final rinse.
Recipe varies by soil type and equipment. PLC stores multiple recipes for different products/equipment. Validated for cleaning effectiveness.
Are CIP systems FDA-validated?
CIP systems can be designed and validated for FDA cGMP compliance. Includes 21 CFR 11 electronic records, audit trails, validated software.
Validation package: IQ (installation qualification), OQ (operation), PQ (performance). Specify validation requirements with RFQ for pharma applications.
Can CIP systems be retrofitted to existing plants?
Yes — mobile CIP skids and modular fixed CIP systems can serve existing plants. Connections required at each cleaning circuit.
Site survey recommended for retrofit. Existing pump/valve/instrumentation can sometimes be reused. Provide as-built drawings.
What chemical dosing is included?
Standard: NaOH (caustic) and HNO3 (nitric acid) automated dosing with concentration verification (conductivity feedback).
Optional: peroxide for sanitization, enzymes for protein soil, surfactants. Chemical compatibility with equipment seals critical — verify with materials list.
What documentation is provided?
Standard: P&ID, electrical drawings, equipment data sheets, control narrative, operator manual, PLC backup, validation protocols.
For pharma: full IQ/OQ/PQ package, software validation, electronic records compliance, training documentation.