Importing animals from non-vendor institutions can often present a heightened risk to the health of your facility. Charles River’s quarantine capabilities allow you to import animals from any source worldwide, without risking the introduction of unwanted pathogens into your own facility. Our state-of-the-art quarantine facilities are equipped with biosecure isolators that provide an excellent quarantine environment. The isolator environment ensures that the health status of your animals is maintained and allows us to accept animals with either adverse or unknown health status. The quarantine period is also an excellent opportunity to permanently archive your line via our convenient sperm cryopreservation option.
As an alternative to traditional quarantine, Charles River also offers a comprehensive colony startup program that is designed to alleviate many of the headaches associated with starting a new animal colony. This program rederives, cryopreserves and rapidly expands your existing colony in just three months, providing security to you and your animal facility and allowing you to begin your research sooner.
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Our study, presented at the 2013 Experimental Biology Conference, focuses on the phenotype and genotype comparison for C57BL/6N substrains contributing to the International Mouse Phenotyping Consortium (IMPC).
Clinical pathology data can assist you in selecting the most appropriate model for your study and can provide important information on the physiology and health of your research animals.
Jun 21–Jun 25
This five-day meeting draws diverse professionals from around the world to share their breakthroughs in the prevention, diagnosis and treatment of diabetes.
Jun 28–Jun 28
Charles River offers a wide range of seminars, workshops and training courses for animal technicians, veterinarians, biologists and laboratory technicians who work with laboratory animals. For more information about our course on animal health monitoring, click "view more" below.
This position is responsible for serving as a as a study director (SD), project scientist (PS) and/or principal investigator (PI) in the direction and execution of assigned studies in compliance with GLP regulations as they apply to the conduct of nonclinical research; coordinating all phases of the study planning process with appropriate departments; generating high-quality project plans, protocols, amendments and reports appropriate for assigned studies; reviewing, interpreting, integrating and presenting data on assigned studies; and functioning as contact for the planning and execution of sponsor interaction related to assigned studies, including proposal management and study scheduling, conduct and reporting.
This position is responsible for managing international aspects of US Federal income tax compliance; assisting with international tax planning, including identification of planning opportunities, designing and implementing plans, and transfer pricing process; overseeing quarterly ETR forecast process; and participating in the tax provision process, including assessment of tax risks, documentation of key positions, and review of non-US tax provision submissions.
Charles River Laboratories, Inc.