HEPA & ULPA Filtration Validation for Cleanroom Environments

Delivering traceable leak detection and efficiency testing for Semiconductor, Pharmaceutical, and Critical Manufacturing, متوافقة تماما مع EN 1822 & ايزو 29463.

Validating HEPA/ULPA Filtration Efficiency and Leak Integrity

Cleanroom operators and filter manufacturers face dual challenges: verifying ISO Class 1–5 cleanliness performance and enforcing 100% zero-leak integrity on every unit. Success depends on rigorous scanning processes while strictly adhering to global EN 1822 و ايزو 29463 standards.

SCPUR bridges the gap between laboratory standards and industrial production scale. We deliver comprehensive solutions, from high-speed automated scanning for standard panels to engineering adaptations for complex geometries, ensuring operational stability and reliable GMP compliance.

Validating HEPA ULPA Filtration Efficiency and Leak Integrity

Industry Challenges & SCPUR Solutions

Transforming manual inspection bottlenecks into automated precision with advanced engineering.

Production QC Bottlenecks-error
Manual scanning is slow, labor-intensive, and prone to fatigue errors. It often fails to match the high throughput of modern 24/7 production lines.
Portable Sensing Technology- SC-8013

High-Speed Automated Scanning: We deploy robotic XYZ-axis scanning with speeds up to 40mm/s, automating 100% of inspections to ensure consistency at mass-production speeds.

Non-Standard Structures-error

Standard probes struggle to maintain consistent sampling on non-standard geometries (e.g., V-Bank, cylindrical), resulting in detection blind spots and incomplete validation.

Non-Standard Structures-check

Flexible Engineering Adaptation: Customized fixtures and multi-axis path planning ensure full coverage for special shapes, eliminating dead zones in compliance with ISO 29463.

Data Traceability Gaps-error

Traditional visual inspection relies on manual paper records, creating disconnected data silos that lack digital integration and fail to meet strict GMP traceability audits.

Smart Visualization & Traceability

Digital Compliance & Visualization: Our software automatically generates 2D/3D leak distribution maps and traceable reports, fully compliant with GMP Annex 1 متطلبات.

Explore The High-Efficiency & Cleanroom Testing Series

Explore The High-Efficiency & Cleanroom Testing Series

Our flagship product line for HEPA & ULPA (H13–U17) validation. Built for both mass production and R&د, this series integrates high-speed automated scanning (up to 40mm/s) with MPPS efficiency testing. It delivers full GMP-compliant traceability for both standard panels and complex filter geometries.

Versatile Solutions Across Critical Industries

Our systems are trusted globally to maintain the highest standards of air purity in specialized environments.

Semiconductor Wafer Fabs

Semiconductor Wafer Fabs

Validates ULPA integrity to ensure ISO Class 1 cleanliness for lithography.

HEPA ULPA Production Lines

Pharmaceutical GMP Facilities

Guarantees zero-leak performance for aseptic lines compliant with GMP Annex 1.

Pharmaceutical GMP Facilities

HEPA/ULPA Production Lines

Automated 100% testing ensures zero-defect shipments at mass-production speeds.

ر&د & Third-Party Testing

ر&د & Third-Party Testing

Flexible fixtures and path planning validate non-standard geometries effectively.

From Subjective Inspection to Automated Quantitative Analysis

A leading manufacturer of H13/H14 HEPA filters for pharmaceutical and electronic industries faced quality bottlenecks. By upgrading to our automated scanning system, they transformed their QC process from experience-based estimation to data-driven precision.
From Subjective Inspection to Automated Quantitative Analysis

The Challenge

Subjective & Inconsistent: Traditional smoke tests relied on operator experience, leading to inconsistent judgements and fatigue errors.

Data Silos & Limitations: DOP methods provided only Pass/Fail results without local data, making precise repairs and auditability impossible.

The SCPUR Solution

Automated Quantitative Scanning: Robotic sampling calculates local efficiency based on standard limits, ensuring 100% repeatability over human inspection.

Closed-Loop Rework Verification: Precise defect mapping enables aDetect–Repair–Confirmcycle, ensuring zero-defect delivery without delays.

Integrated Performance Monitoring: Simultaneous pressure drop measurement prevents over-sealing during repair, ensuring optimal aerodynamic performance.

evaluate 1

Reliable quality control is not only about detecting leaks, but making the detection actionable and verifiable. By upgrading to quantitative scanning, we have transformed specific experience into a sustainable, auditable engineering process.

Full Lifecycle Support Beyond The Hardware

Custom Engineering Integration-4

Custom Engineering Integration

We adapt software interfaces and fixture dimensions to seamlessly integrate our systems into your specific production environment.

Professional System Commissioning

Professional System Commissioning

Our engineers provide installation guidance and comprehensive training to ensure immediate operational proficiency.

ISO Calibration And Maintenance

ISO Calibration And Maintenance

Stay audit-ready with annual calibration services and rapid spare parts supply to minimize downtime and guarantee data validity.

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مخصص ر&د & حلول مخصصة

مخصص ر&د & حلول مخصصة

الامتثال للمعايير العالمية

الامتثال للمعايير العالمية

100% نظام برمجي مطور ذاتيًا

100% نظام برمجي مطور ذاتيًا

المعايرة عن بعد & الدعم العالمي

المعايرة عن بعد & الدعم العالمي

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