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qlabs-legionella-infections

Healthcare Facilities Pose Particular Risk of Legionella Infections

Responding to a Centers for Disease Control and Prevention (CDC) report indicating Legionnaires’ Disease (LD) kills 25% of those who are infected while getting treatment or residing in a healthcare facility, the Department of Health & Human Services, Centers for Medicare & Medicaid Services (CMS), on June 2, 2017, released a memorandum entitled, “Requirement to

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qlabs-purchases-buildings

Q Laboratories Purchases Buildings

Q Laboratories has purchased two buildings (1920 and 1930 Radcliff Avenue, Cincinnati, Ohio) as part of their ongoing capacity expansion project. The two buildings sit adjacent to the 30,000 sq. ft. laboratory building currently under construction, scheduled to be completed in Spring 2018. The newly-acquired buildings entail 25,000 sq. ft., and will eventually serve as

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qlabs-method-verification

When Do I Need a Method Verification?

In this age of the Food Safety Modernization Act (FSMA) it is increasingly important that the methods you (or your third-party lab) are using are validated by a recognized organization. Methods contained in the FDA Bacteriological Analytical Manual (FDA-BAM), the USDA-FSIS Microbiology Laboratory Guidebook, as well as methods approved by independent, non-governmental bodies such as

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qlabs-summertime-weather

Summertime Weather Turns Consumers’ Thoughts to Sunscreen

As the weather warms and the sun peeks out from behind the clouds, thoughts turn to outdoor activities and enjoying the pleasant weather. What follows is the inevitable need for sunscreen/sunblock products to help keep consumers and their families safe. This requires sunscreen product manufacturers to perform due diligence to assure the products they place

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qlabs-minimum-inhibitory

Minimum Inhibitory (MIC) and Minimum Bactericidal Concentration (MBC) Evaluations as R&D Tools

Q Labs Offers MIC Testing & MBC Testing for Product Formulation MIC Definition & Purpose The Minimum Inhibitory Concentration (MIC) is defined as the lowest concentration of an antimicrobial ingredient or agent that is bacteriostatic (prevents the visible growth of bacteria). MICs are used to evaluate the antimicrobial efficacy of various compounds by measuring the

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qlabs-env-monitoring-photo

Environmental Monitoring Design Utilizing the Zone Concept

With the implementation of the Food Safety Modernization Act (FSMA), as well as the recently released FDA Guidance on controlling Listeria monocytogenes in RTE foods, it is more important than ever to have a carefully designed, robust Environmental Monitoring (EM) program in your food manufacturing plant. Effective design of your EM program is essential to

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qlabs-3-day-yeast-and-mold-results

Q Laboratories, Inc. Now Offers 3-day Yeast and Mold Results

Q Laboratories, Inc. is excited to offer our clients faster turn-around times for their Yeast and Mold testing. Utilizing the Biomerieux TEMPO® YM Assay, results that used to take five days can now be turned around in three.  TEMPO® YM is an official AOAC Research Institute Performance Tested Method for numerous matrices including, cheese, yogurt,

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Q Laboratories, Inc. Gains International Recognition-Joins Elite Group of Expert Laboratories

Q Laboratories, Inc. (Cincinnati, Ohio) has been named an AFNOR Certified Expert Laboratory, thereby qualified to perform validation studies on instruments, test kits and materials for the food microbiology testing industry in France. Representatives of Q Laboratories, Inc. were in Paris, France the week of January 22nd to present before the Association Française de Normalisation

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Nontuberculous Mycobacteria (NTM) infections associated with heater-cooler devices

In the last few years, the FDA has focused on increasing awareness of Nontuberculous Mycobacteria (NTM) infections associated with heater-cooler devices and the subsequent risks to patients in health care facilities.  The FDA reports that there were 32 reports of infections associated with heater-cooler devices or bacterial heater-cooler device contamination between 2010 and 2015, but

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Reprocessing of Reusable Medical Devices

The FDA requires manufacturers of reusable medical devices to provide reprocessing instructions that ensure that the device can be used safely and for the purpose for which it is intended. Developing and validating these instructions can be a complex and highly specialized activity. Guidance on this process can be found in a document created by

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