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Preclinical Sites At-a-Glance
Montreal and Sherbrooke, Canada
Canada is home to two Charles River Preclinical Services facilities: one in Montreal, and the other less than two hours away in Sherbrooke.
One of our largest facilities, Charles River Montreal offers routine toxicology and various specialized services, such as inhalation and infusion toxicology, bone research and genetic toxicology. Also offered is a wide range of laboratory-based services, including metabolism and pharmacokinetics, immunology, imaging and molecular biology, as well as preclinical and clinical bioanalytical chemistry.
Our Sherbrooke facility functions as an extension of the Montreal facility. Designed to mirror operations in Montreal, Charles River Sherbrooke can provide a full spectrum of toxicology services as well as required laboratory and pathology support services. Housing compliant with the European Directive 2010/63/EU is available for small and large animals.
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Posters & Researchers (Available only in The SourceSM)
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Charles River Laboratories International, Incorporated
251 Ballardvale St.
Wilmington, MA 01887
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Blood sampling for clinical pathology assessment in mice has always been a challenge, given the limited amount of blood that can be collected both at necropsy and particularly during the live phase of a study. To address this difficulty, and in keeping with our commitment to the 3Rs (replacement, reduction, refinement), Charles River has developed and validated a method permitting a 75% reduction in the total blood volume required for hematology and clinical chemistry assessments in mice. Learn more.
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Introducing Capillary Microsampling

 Many toxicologists and regulators view the mouse as the toxicology model of last resort. Traditional analytical methods and study designs have not allowed for the direct correlation of toxicological effects with drug exposures within the same mouse. Each analysis endpoint (other than pathology) requires blood samples that are a relatively large fraction of the mouse's total blood volume. Consequently, mouse toxicology designs have required the endpoints to be dispersed among large numbers of satellite groups. While covering all standard endpoints required for human drug toxicology, these studies have produced a less-than-satisfactory collage of data.
The advent of new mass spectrometers has meant that instrument sensitivities have increased dramatically, and this, along with the introduction of new endpoints for immunoassay (e.g., MSD), permits the use of the reduced sample volumes without losing assay sensitivity. Learn more.
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DART Studies in Guinea Pigs
The scientific and technical staff within our Pennsylvania facility have successfully researched and developed an alternate repeat-dose oral gavage technique that can be utilized in guinea pigs. This technique is now available for use in multiple study designs, including general toxicology assessments and DART studies. Learn more.
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Using Quantitative Whole-Body Autoradiography (QWBA) to Investigate Whole-Body Tissue Distribution in the Minipig
QWBA is a powerful tool in determining the relative tissue distribution of radiolabelled drugs. This technique, which provides data on the whole-body distribution, can also be used to determine distribution of drugs to specific tissues and localization within target tissues. It is, however, usually restricted to the investigation of distribution in smaller species. In the study described in this poster, the tissue distribution of radioactivity was investigated in the minipig using QWBA techniques. This appears to be the first application of QWBA for this investigation type.
Click here to view our poster on QWBA to learn more.
Click here to listen to our podcast on QWBA.
(Poster and podcast are only available in The SourceSM. Click here to register.)
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Physicochemical Testing Now Also
Available in North America
 Charles River is pleased to announce that physicochemical testing services will now be offered at both our Edinburgh, UK and Ohio, USA preclinical facilities. Physicochemical testing is integral to meeting the requirements of product registration for pharmaceuticals, agrochemicals, biocides, chemicals and veterinary products. This work is typically performed in the early stages of testing, often in conjunction with genetic and acute toxicology testing. This new testing initiative is housed in a purpose-built laboratory outfitted with equipment dedicated specifically to physicochemical testing. Learn more. |
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mypreclinicalSM
Our new and improved global portal, mypreclinicalSM, offers customizable solutions and increased functionality for secure study tracking. Now available at all of our preclinical facilities. Learn more.
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