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JRF Global - An international Preclinical CRO
JRF Global is a GLP and AAALAC accredited pre-clinical CRO with the presence in US, Japan, India, UK, Canada, Spain, and China.
In 25 years of OECD GLP compliance, over 43,000 of our GLP reports have been well received by Global regulators like FDA, EMA, EPA, ECHA, Japan etc. All studies conducted at JRF Global are in accordance with the regulatory requirements of the EMA, US FDA, ICH, OECD, JMAFF, ISO and OPPTS etc.
Our IND-enabling safety assessments include Mammalian Tox, Repeated dose Inhalation, Developmental and Reprotox, Genotox, Immunotox & Neurotoxicity, Carcinogenicity, EDSP, ADMET / DMPK, in vitro tests, in vitro DMPK, and Discovery and Development research.
In addition to Toxicology, JRF also offers Custom synthesis, Eco-toxicology, Chemistry, Environmental Fate and Metabolism, and other regulatory testing requirements.
To know more about us, stop by our Booth # 101 and enjoy the conversation with our scientists.
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