Baie-D'urf, QC
Established in 1989, ITR Laboratories is one of the newer contract research laboratories in North America and has successfully conducted a significant number of preclinical studies.
The ITR studies are fully GLP (Good Laboratory Practices) compliant with protocols designed to allow our clients to meet the specific regulatory requirements where the products are to be marketed.
ITR conducts general toxicology, intravenous infusion, interaction studies, cardiovascular profiling/safety studies and ADME studies with or without radiolabelled substances (pharmacokinetics, excretion and mass balance, autoradiography analysis, quantitative and qualitative tissue distribution). ITR conducts preclinical studies in rodents, dogs and primates.
ITR has assembled a staff of professionals, technicians and scientists, with direct long term experience in toxicological assessments. The company has grown steadily with clients throughout North America, Europe and Japan.
The present facility (19 animal rooms) is equipped to undertake a wide range of toxicity studies with a particular expertise in intravenous infusion (some of ITR's personnel have over then years experience in this area).
The modern facilities include surgical and cardiac profiling units, as well as a fully integrated toxicology and pathology laboratory.
The laboratory has been inspected and approved by AAALAC, CCAC and the FDA. The entire facility is purpose-built and state-of-the-art.
19601 Clark-Graham Ave.
Baie-D'urf, QC H9X 3T1
CA
19601 Clark-Graham Ave.
Baie-D'urf, QC H9X 3T1
CA
Legal Name: ITR Laboratories Canada Inc.
Number of Employees: 110
Title: Vice President
Area of Responsibility: Management Executive
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Title: President
Area of Responsibility: Management Executive
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Title: Vice President
Area of Responsibility: Management Executive
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Title: Supervisor, Business Development
Area of Responsibility: Domestic Sales & Marketing
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Title: Manager
Area of Responsibility: Manufacturing/Production/Operations
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ITR (International Toxicology Research) Laboratories, an ultramodern facility situated in the western section of Montreal island, conducts comprehensive nonclinical studies for the pharmaceutical and biotechnology industries. These include:
general toxicity, specialized intravenous or subcutaneous infusion studies (up to 26 weeks in duration), special clinical pathology, ADME/pharmacokinetic evaluations, cardiovascular profiling and pathology. Our facilities are FDA-audited and include a surgical and cardiac profiling unit as well as a fully-integrated toxicology and pathology laboratory.
We are in the process of completing our second expansion with another six animal rooms to be completed next month, bringing our total number of rooms to 25.
We are qualified to undertake a wide range of toxicity studies and have particular expertise in intravenous infusion studies. Every study conducted at ITR complies with Good Laboratory Practices (GLP). We work in conjunction with our sponsors' monitors to assure that all aspects of the study conduct are in accordance with the study protocol.
621510
Japan, United Kingdom, United States