Experience what Q can do for you!
We have served the Food Ingredients/Flavorings, Cosmetic, Pharmaceutical, OTC, Health and Beauty Care and Dietary Supplement industries since 1966, offering comprehensive microbiology and chemistry product analysis and research and development services.
Registered with the FDA for pharmaceutical testing (Reg. #1527260), cGMP/GLP Compliant and ISO/IEC 17025 Accredited, Q Laboratories can help you maintain the high level of excellence you demand for your products. An independent laboratory, combining state-of-the-art technology with personal service and attention, Q Laboratories can provide services to meet all your testing and quality assurance needs.
For over 50 years, Q Laboratories has maintained excellence in science as well as customer satisfaction, creating a level of confidence and trust among clients that is unparalleled.
Your ultimate goal as a manufacturer is to sell products. The most effective way to sell products is to have the most conclusive, comprehensive information about those products. That is where the Q Laboratories Analytical Chemistry Laboratory comes in, providing the information you need!
Q Laboratories can provide a wide range of Microbiology Laboratory Services. Whether you need a basic enumeration for bacterial presence, screening for specific pathogens, or a computerized microbial identification, our professionals can provide these services for you.
At Q Laboratories we understand your laboratory needs do not always follow compendial guidelines or previously determined methodology. We offer versatility in our services in case you need to operate
“outside the box.”
What is the ELAP Certification and why is it important? We are happy to announce that Q Laboratories is now approved by the New York State Department of Health’s Environmental Laboratory Approval Program (ELAP). New York ELAP approval is required in New York as part of the Protection Against Legionella regulation which was passed in July, 2016. This
Bactericidal Considerations to the FDA Briefing Document As you may or may not have heard, the FDA has released a Briefing Document in March of 2020 that proposes an alternative organism panel from the Tentative Final Monograph (TFM) for consumer and healthcare antiseptics. Amongst growing interest from our clients on this topic, we have authored
Raw Material Testing for Material Identity, Purity and Quality Are you in need of a raw materials testing partner? Are you in the process of qualifying new material suppliers for your supply chain, and need raw materials testing? Raw Material Testing & Analysis Registered with the FDA for pharmaceutical testing (Reg. #1527260), cGMP/GLP Compliant and
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Cincinnati, Ohio 45204-1823
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