HEPA Filter Certification for Critical Laboratory Equipment
Common Equipment We Test:
- Biosafety Cabinets (BSCs) – Class I, II, and III cabinets for research and pharmaceutical applications [1]
- Laminar Flow Workstations & Hoods – Horizontal and vertical flow devices for sterile compounding and cleanroom operations
- Cleanroom Systems – Buffer rooms, ante rooms, and ISO-classified controlled environments
- Isolators & Containment Systems – CAI, CACI, and pharmaceutical isolators for sterile and hazardous drug compounding
- Animal Transfer Stations – Ventilated cage change stations for research facilities
- HEPA & ULPA Filter Banks – Rooftop and in-line filtration systems for supply and exhaust air

Protect Your Critical Environment with Expert HEPA Filter Certification & Testing
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Industries We Serve
Manufacturing & Industrial
- Pharmaceutical manufacturing
- ISO classified cleanrooms
- Food processing facilities
- Aerospace and aviation
- Petrochemical facilities
- Metallurgical operations
Healthcare & Medical
- Hospital operating rooms, laboratories, and pharmacies
- Inpatient compounding pharmacies
- Independent sterile compounding facilities
- Radiopharmaceutical facilities
- Oncology clinics
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- FDA facilities
- FBI laboratories
- Crime and forensic laboratories
- Government research entities
Education & Research
- Colleges and universities
- Independent research laboratories
- BSL-2 and BSL-3 containment facilities [2]

Why Trust Allometrics for HEPA Filter Certification & Testing

Our HEPA Filter Certification & Testing Process
What is HEPA Filter Testing?
Benefits of Professional HEPA Filter Certification
Maintain Regulatory Compliance – Stay audit-ready with detailed documentation that proves your filtration systems meet your industry-specific requirements.
Protect Critical Operations – Prevent contamination that could ruin pharmaceutical batches, compromise sterile compounding, or invalidate research results.
Ensure Personnel Safety – Verify that the containment systems protecting your team from hazardous materials and biological agents are functioning properly.
Avoid Costly Failures – Catch filter problems before they result in product recalls, failed batches, workplace exposure incidents, or regulatory findings.
Extend Equipment Life – Identify issues early before they cause expensive system damage or necessitate emergency replacements.
Risks of Neglecting HEPA Filter Testing
Failed Audits – Without documented filter integrity testing, you’re vulnerable to regulatory findings that can halt operations.
Undetected Contamination – Compromised filters may seem normal while allowing contaminants into your cleanroom or lab, potentially invalidating months of work.
Product Loss & Recalls – Contaminated batches mean destroyed inventory, damaged reputation, and potential legal liability.
Personnel Exposure – When containment fails, workers may be exposed to hazardous materials without realizing it until health effects appear.
Common Questions About HEPA Filter Certification & Testing
- https://www.nsf.org/knowledge-library/biosafety-cabinetry-certification
- https://www.cdc.gov/labs/pdf/SF__19_308133-A_BMBL6_00-BOOK-WEB-final-3.pdf
- https://www.fda.gov/regulatory-information/search-fda-guidance-documents/sterile-drug-products-produced-aseptic-processing-current-good-manufacturing-practice
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- Service Inquiries
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