JRF Global

Exhibitor

JRF Global offers comprehensive non clinical GLP research services for worldwide regulatory submissions.

We offer fast, transparent, cost-effective and hassle-free services in Toxicology, Chemistry, Bioanalysis, various Immunological Assays, and other regulatory testing requirements. Our experienced and knowledgeable scientists have worked with pharmaceutical and biopharmaceutical, agrochemical, vaccine industries and veterinary products.  With locations in India, USA, and Japan, we are the partner-of-choice of over 600 companies for generating safety data.

We endeavor to develop tailor made protocols based on the unique properties of your molecules to satisfy any specific regulatory requirements. All the laboratories of JRF Global are fully compliant with OECD Good Laboratory Practice (GLP) accreditation.

The most critical criterion for the pre-clinical studies are study updates and time line compliance. Our scientific team and professional project department have expertise to minimize the time and also to accelerate the studies in order to save time. We also provide timely updates of the projects to the sponsors.

With an exceptional quality and timely delivery of reports at very competitive prices as compared to the western labs, JRF Global is the right choice as your preferred partner for your IND / NDA / ANDA registrations.

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