Component Testing You Can Trust

Our lab facilities are purpose-built to assess asset performance and investigate component failures, supporting clients with both pre-deployment validation and in-service troubleshooting.

Our Capabilities:
  • Accelerated life testing
  • Failure root cause analysis
  • Factory Acceptance Testing (FAT) & Site Acceptance Testing (SAT)
  • Cleanroom valve testing, overhaul, and repair

Accelerated Life Testing

Our biopharma process-emulation platform allows us to simulate real operating conditions and assess long-term performance in a compressed time frame. This is ideal for:

  • Generating validation data for new components
  • Supporting product qualification and regulatory submissions
  • Evaluating component reliability under site-specific conditions
  • Identifying early failure modes and performance degradation
Why SCRI-IS?
  • Purpose-built reliability test platform for life sciences applications
  • Simulates real-world CIP/SIP cycles and process conditions
  • Supports vendor benchmarking and material validation

Failure Root Cause Forensic Analysis

When components fail in service, our forensic analysis methods uncover the root cause. This includes:

  • Physical analysis of material degradation
  • Comparison of failed vs. virgin samples
  • Detection of process or installation-related failure triggers
Why SCRI-IS?
  • Deep expertise in life sciences failure modes and mechanisms
  • Cleanroom lab with full material testing capability
  • Trusted by global manufacturers for failure investigations

Factory Acceptance Testing (FAT) & Site Acceptance Testing (SAT)

We support clients in ensuring the compliance, functionality, and integrity of equipment and systems before and after installation. Our FAT and SAT services are tailored to:

  • Validate systems against site-specific specifications and global standards (e.g., ASME BPE, DIN)
  • Verify mechanical, control, and documentation readiness pre-installation
  • Conduct SATs on-site to confirm installation integrity and operability in actual process conditions
  • Identify and resolve non-conformances early in the commissioning cycle
Why SCRI-IS?
  • Independent third-party validation aligned with industry and site standards
  • Experience with biotech manufacturing systems and GMP-critical assets
  • Reduces delays during commissioning and handover

Cleanroom valve testing, overhaul, and repair

Our cleanroom-grade mechanical workshop is purpose-built for life sciences clients requiring high standards of valve reliability and compliance. We inspect, overhaul, and refurbish critical valves—especially Pressure Safety Valves (PSVs)—with precision and care.

Services include:
  • Full disassembly and inspection of PSVs and control valves
  • Cleaning, refurbishment, and replacement of worn parts
  • Functional and performance testing under simulated process conditions
  • Calibration and documentation to support regulatory requirements
Why SCRI-IS?
  • Rigid cGMP-compliant processes backed by a robust QMS
  • Comprehensive valve lifecycle support from inspection to commissioning
  • Trusted by top-tier manufacturers for critical valve reliability services

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Preventing Downtime in Biopharma Plants

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News
June 9, 2023

Elastomer & Valve Community of Practice (CoP) Event

SCRI-IS Technologies, in association with Engineers Ireland MEETA Asset Management Society, recently hosted the inaugural Elastomer & Valve Community of Practice (CoP) event at our facility in Glasnevin. The thought-provoking…
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News
January 13, 2023

Minimizing Machine Downtime for Life Sciences Industry and Their Patients

Machine downtime is a major disruption to production and can have a significant impact on manufacturing facilities. Downtime increases costs, leads to missed targets, and in the sectors of biotechnology,…
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Articles
January 10, 2023

Transitioning Pharmaceutical Companies From ‘Fast Followers’ to ‘First Adopters’

In recent decades, there have been rapid advancements in technologies. These advancements have filtered down to many sectors and industries, however, the pharmaceutical industry can be slow to adopt these…
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