VaLogic Bio supports biotech, pharma, and life sciences organizations that depend on maintaining strict environmental controls. Our compliance support services are designed to meet rigorous standards (IEST -RP-CC034, CAG-003, GMP ), which require ongoing documentation of air filtration performance.
Air quality and filtration are just one of the many elements in your overall compliance strategy. HEPA filters are designed to trap airborne particulates, protecting sensitive research and the lab environment. If they fail, it puts your facility operations, products, and personnel at risk.
Testing confirms that each filtration unit is installed correctly and operating within specification, capable of trapping airborne particles at the required threshold.
HEPA filter testing protocols use DOP (dioctyl phthalate) or PAO (polyalphaolefin) challenge agents to simulate contamination. After introducing them into the test environment, we use photometers to scan the filters and identify potential leaks or installation flaws.
Testing frequency depends on your facility type and risk classification. High-risk labs and environments subject to rigorous GMP or ISO controls typically conduct tests every 6–12 months. Retesting is also recommended after filter replacements, renovations, or system malfunctions.
Testing confirms performance, but certification provides the documented proof. A HEPA filter certification from VaLogic includes a comprehensive report with equipment readings, scan data, and technician notes. All certificates are traceable, audit-ready, and aligned with your organization’s SOPs.
VaLogic Bio has supported more than 400 biotech companies since 2001. We’re veteran-founded, process-oriented, and laser-focused on helping your teams stay audit-ready without slowing you down.
We customize our services to your specific environment, risk profile, and regulatory requirements. And when it comes to communication, we’re known for speed and transparency. Our experts are easy to reach and respond quickly, so your team is always on top of scheduling, results, and next steps.
HEPA filter certification is just one piece of the puzzle. Our GxP advisory and compliance services include everything you need to stay on top of regulatory standards while achieving your organizational goals at pace:
VaLogic Bio has supported more than 400 biotech companies since 2001. We’re veteran-founded, process-oriented, and laser-focused on helping your teams stay audit-ready without slowing you down.
We customize our services to your specific environment, risk profile, and regulatory requirements. And when it comes to communication, we’re known for speed and transparency. Our experts are easy to reach and respond quickly, so your team is always on top of scheduling, results, and next steps.
HEPA filter certification is just one piece of the puzzle. Our GxP advisory and compliance services include everything you need to stay on top of regulatory standards while achieving your organizational goals at pace:
Most HEPA filter tests are completed within a half-day to full-day timeframe, depending on the number of units and lab complexity.
We plan around your workflow. Services can be performed during off-hours or scheduled downtime.
You’ll receive immediate feedback, a fail report, and remediation recommendations. VaLogic will also support retesting after repairs or replacements.
Ready to ensure your lab meets regulatory standards without the headache? VaLogic Bio makes HEPA filter testing straightforward, timely, and compliant.
