What we do
Tailored compliance for critical environments.
Providing specialized cleanroom qualification, equipment validation, and expert microbiological consultation designed to meet strict international standards.
Specialized services for high‑precision sectors.
We deliver tailored compliance and contamination control strategies for your workflows. From equipment qualification including CSV to sterile and depyrogenated laboratory consumables, we ensure your operations achieve absolute regulatory alignment.
Pharmaceutical
Pharmaceutical GMP & Investigation Services
Comprehensive compliance, risk management and validation frameworks for sterile and non-sterile drug manufacturing facilities.
- ISO
- USFDA
- EMA
- PIC/S
- Drugs and Cosmetics Act
End-to-end design, gap analysis and execution aligned with current international mandates.
Deep-dive root-cause identification for environmental monitoring (EM) excursions, deviations, operational failures and out-of-specification (OOS) results.
Specialized intervention, analysis and robust remediation plans for media fill failures.
Meticulous qualification protocols for Purified Water (PW), Water for Injection (WFI), clean utilities and HVAC systems.
Qualification of equipment, including Computer Systems Validation (CSV).
Comprehensive pre-inspection plant assessments to prepare for successful audits by global regulatory bodies.
Clear, technically sound and fully compliant laboratory procedures and execution scripts.
Specialized training structures that reduce laboratory subjectivity and human error.
How a microbial failure investigation runs
From the first excursion to a CAPA your inspector can follow.
- Excursion, deviation or OOSAn EM excursion, operational failure, media fill failure or out-of-specification result.
- Root-cause identificationA deep-dive investigation into what actually went wrong, backed by microbiology.
- CAPA implementationCorrective and preventive actions, with robust remediation plans that hold up in an audit.
Cleanroom for Semiconductor and PharmaSuticals
Precision Cleanroom Qualification & Testing
Advanced environmental monitoring, structural integrity assessments and particle dynamic testing, tailored to meet stringent semiconductor manufacturing standards.
Select a test to see which part of the cleanroom it checks.
Airborne particle count
Measures suspended air particles with calibrated counters to verify the target cleanliness class.
Supply
Laboratory Consumables and Equipment
Supply of high-calibre sterile and depyrogenated consumables, and laboratory testing instruments tailored for pharmaceutical QC environments.
View consumables & equipmentSupply of consumables
Reliable distribution of premium sterile, non-sterile and depyrogenated microbiological consumables. All consumables meet the applicable regulatory requirements.
Equipment supply and custom design
Sourcing, supply and custom engineering of specialized pharmaceutical QC laboratory instruments, built around your exact requirements.