BioReliance is a focused and specialized provider of toxicology services that can speedily move your product from discovery to market. We have been a scientific leader in toxicology for more than 65 years – from safety testing the first polio vaccines in the 1950’s, to validating new transgenic mouse models for carcinogenicity testing, and most recently advising, qualifying and validating new assays and designs to meet updated and new OECD guidelines.
BioReliance concentrates on providing niche services and innovative assays to address product discovery through screening assays, and product development and carcinogenicity assessment through GLP regulatory submission assays. BioReliance services include a broad spectrum of in vitro and in vivo toxicology testing services designed in accordance with international guidelines and are conducted in full compliance with GLP regulations. We have experience offering standard assays and accepted designs, while employing a scientific team integrally involved in new design development and acceptance. Our expertise uniquely qualifies us to custom design testing strategies even when they involve new or novel products. These services are provided to producers of traditional pharmaceuticals, biopharmaceuticals, medical devices, gene therapies, industrial chemicals and consumer products. Our 50,000 square foot, state-of-the-art facility and dedicated staff continue to lead and advance the field of toxicology with the implementation of the latest technologies that help clients register products internationally.
Our areas of expertise include:
BioReliance offers comprehensive genetic toxicology services for the detection of toxic, mutagenic, clastogenic, and morphological transforming activity in a number of well-characterized test systems.
BioReliance offers analytical services in support of toxicology studies including, method validation, formulation analysis, homogeneity and stability testing.
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