Allometrics combines 50 years of cleanroom certification expertise with A2LA ISO 17025 accredited instrument calibration—ensuring every airflow measurement, particle count, and pressure differential reading you receive is backed by NIST-traceable accuracy. Our CETA Registered Cleanroom Certification Professionals and NSF Accredited Technicians provide comprehensive environmental testing across all regulatory standards—from compounding pharmacies to sterile manufacturing—backed by nationwide service and documentation that satisfies even the most rigorous audits.
Comprehensive Cleanroom Testing Backed by 50 Years of Expertise
Five Decades of Multi-Industry Regulatory Expertise
- Experienced technicians conducting testing across pharmaceutical, healthcare, food processing, aerospace, and research environments since 1976
- A2LA ISO 17025 accredited calibration laboratory ensures all testing instruments maintain NIST-traceable measurement accuracy
Nationwide Service with Consistent Quality
- Consistent testing protocols and documentation formats across all locations
- Rapid response capabilities that minimize operational disruption
- Single provider for equipment certification, instrument calibration, and environmental monitoring
- Online portal for fast and easy documentation access
Expert Cleanroom Certification for Every Application
USP 825 Cleanroom Certification
Radiopharmacy operations demand environmental certification that accommodates hot cell configurations, radiation safety protocols, and time-sensitive compounding—specialized testing that requires understanding nuclear medicine workflows. Our field service teams deliver complete USP 825 compliance verification for nuclear pharmacies, hospital departments, and specialty clinics nationwide. Explore our USP 825 certification services →
USP 797 & 800 Cleanroom Certification
Sterile compounding environments require testing that verifies air quality, pressure differentials, and environmental controls meet patient safety and worker protection standards. We perform complete certification of primary engineering controls, buffer rooms, anterooms, and hazardous drug areas—from HEPA filter integrity testing to airflow visualization studies—with documentation formatted for regulatory inspections and accreditation surveys. [1] See complete USP 797 & 800 testing capabilities →
Media Fill-Kits
Aseptic technique validation across pharmaceutical compounding, sterile manufacturing, and healthcare applications doesn’t require scheduling technician visits—our ready-to-use kits arrive with everything needed for low, medium, and high-risk procedure testing. Complete the simulated compounding at your convenience, return samples with prepaid shipping, and receive detailed pass/fail analysis formatted for audit readiness. Learn about media fill validation programs →
Gloved Fingertip Sampling
Visual observation of garbing procedures can’t detect the contamination that gloved fingertip sampling reveals—making it the objective verification method regulatory standards require for personnel competency qualification and routine monitoring. Our contact plates and laboratory analysis provide documented proof that personnel maintain proper aseptic technique during sterile preparation activities across pharmaceutical, healthcare, and manufacturing environments. Discover gloved fingertip sampling solutions →
Monthly Surface Sampling
Microbial contamination establishes itself on equipment surfaces and high-touch areas long before visible problems appear—making monthly surface sampling your early warning system. Choose self-collection kits or onsite technician visits, both delivering consistent laboratory analysis with CFU count reports that document your environmental monitoring program. Review monthly sampling program options →
Sterile Compounding Pharmacy Services
Beyond certification testing, comprehensive environmental monitoring includes viable air sampling, temperature/humidity validation, pressure differential verification, and automated monthly sampling programs. We support independent pharmacies, hospital operations, and radiopharmacies with the complete range of services required for sterile compounding compliance resulting in care tailored to each patient’s needs. [2] View all sterile compounding services →
Schedule Your Cleanroom Certification Today
Don’t wait until your next audit creates unnecessary pressure. Call (281) 474-3329 to schedule certification testing with nationwide service, CETA-registered technicians, and documentation that satisfies the most rigorous regulatory inspections.
Cleanroom Certification and Testing: Common Questions Answered
The cleanroom certification process involves comprehensive environmental testing to verify your controlled environment meets regulatory standards. We measure airflow patterns, conduct particle counts, verify pressure differentials, perform HEPA filter integrity testing, and other services. All measurements use calibrated instruments with NIST-traceable accuracy, and we provide the documentation necessary for regulatory inspections and accreditation surveys.
Cleanroom certification services are provided by specialized environmental testing companies with trained technicians and proper instrumentation. We employ CETA Registered Cleanroom Certification Professionals and NSF Accredited Technicians who have completed specialized training in controlled environment testing. Our A2LA ISO 17025 accredited calibration laboratory ensures all testing instruments maintain the measurement accuracy regulatory standards require for pharmaceutical, healthcare, and manufacturing applications.
Resources
- https://www.pharmacytimes.com/view/protecting-pharmacy-technicians-key-practices-in-hazardous-drug-compounding
- https://www.bizjournals.com/southflorida/news/2026/01/07/compounded-medications-cleveland-clinic-benefits.html