Los Angeles Clean Air Device Certification

Biopharmaceutical and medical related research laboratories throughout Los Angeles rely on the team at GL Technologies to provide testing and certification of their clean air devices. We provide on-site services help our clients' facilities meet the requirements of IEST-RP-CC002 and the manufacturers specs. Our certification services will help your orgnaizaiton meet strict regulation requirements and maintain product quality.Organizations both large and small in a wide variety of research laboratories rely on GL Technologies for not only clean air device certification, but biosafety cabinet certifications, fume hood, and much more!

To speak with the experts about your clean air device needs, please fill out our online form or give us a call!

858-202-1408

Clean Air Device Testing

(Depending on the type of device)

Inflow Velocity

Inflow velocity testing provides valuable information about how air filtration systems are performing. By quantifying the speed when air enters the device, the technicians at GL Technologies will be able to test the device's ability to capture and remove airbone contaminants. This testing procedure involves specialized instruments that will measure the rate at which air flows in to the device, usually expressed in cubic feet per minute (or meters per second). With the measurements being taken, we will be abel to have a full evaluation of the airflow performance for your laboratory or facility.

Air Changes

When testing for air changes, this refers to the number of times the air in a given space is repalce with fresh air per hour. The metric helps to evaluate how the clean air device works for removing polluntants while keeping a healthy indoor environment. Researchers and laboratory workers can then assess the performance of clean air technologies that include air purifiers and ventilation systems. With testing and evaluation, GL Technologies will help to implement clean air solutions for both workers and the overall organization.

Filter Integrity (Leak Scan) Testing

Filter integrity testing, also known as leak scanning, is important for clean air devices. The testing involves the evaluation of air flitration systems ability to prevent leaks and keep the air contaminated. When GL Technologies tests the clean air devices we will conduct leak scans, which will identify any leaks or issues with the filtration system, of course, which would compromise the ability of the device to remove contaminants and maintain clean air in the facility. Our taem will be able to detect and fix any flaws in the filter integrity, which will will make sure your equipment is reliable.

Non-Viable Airborne Particle Concentration

Non-viable particle testing is refers to the # of particles supsended in the air that are not capable of reproducing (dust, smoke for examples). The GL Technologies team will evaluate the non-viable airoborne particle concentration to determine if it allows the device to eb effective. This will reduce harmful particles and keep clean standars in the laboratory. With the right measuring and analysis, researchers will have reliability the air devices are performing as needed and promoto a healthy environment in the laboratory or facility.

GL Technologies and Certification

With over 40 years experience working in the biopharmaceutical environment helping companies to maintain compliance and provide certification, our team is ready to perform on-site services for all your organizations needs.

The Basics

Clean air device certification is a systematic process that verifies the performance, safety, and compliance of these devices with industry standards and regulations. Certification is typically carried out by accredited third-party organizations or in-house quality teams with specialized expertise.  GL Technologies has extensive experience in clean air device certifications for clients throughout the Los Angeles region.

Key aspects of clean air device certification include:

Performance Testing

Performance testing evaluates the device's ability to maintain specific environmental conditions, such as particle counts and air velocity, within defined tolerances. This validates that the device can create and maintain a clean and controlled environment as required for biopharma and pharmaceutical processes.

Biological Safety

For devices used in handling biological agents, certification includes testing to confirm their ability to provide containment and protection to operators and the environment. This is particularly crucial when working with hazardous materials or organisms.

Industry Compliance

Certification ensures that clean air devices comply with relevant industry standards and regulations, such as ISO 14644 for cleanrooms and ISO 9001 for quality management systems. Compliance with these standards is required for regulatory approval and international trade.

Regular Maintenance

Clean air devices must be regularly maintained and monitored for continued performance. Certification may require a schedule for maintenance and calibration to guarantee consistent results.  GL Technologies works with our clients to set up a maintenance schedule to keep keep instruments properly working and compliant with industry regulations.

About GL Technologies

GL Technologies (formally Calibration Consultants) is a full service calibration provider specializing in the Biopharmaceutical and Medical Device industries. Our management has worked in, managed, and developed FDA cGMP fully compliant programs. Our services include roving crews for the Biopharmaceuticals for regular scheduled calibrations or shutdown and new system situations. GL Technologies also places qualified individuals on various large and small Biopharmaceutical and Medical Device companies. The services we provide include general Calibration/ Metrology support, asset and CMMS management, compliant program development, SOP development, and maintenance/ facilities support.

To speak with the experts about your clean air device needs, please fill out our online form or give us a call!

858-202-1408