Established in 2011, Liveon Biolabs Pvt. Ltd. is a premier OECD-GLP certified Contract Research Organization (CRO) based in Tumakuru, Karnataka, India. We specialize in delivering comprehensive preclinical/non-clinical research services. We strive to support the development and product registrations of pharmaceuticals, medical devices, agrochemicals, and more for global markets. We offer testing in compliance with many international regulatory bodies including FDA, Europe MDR, Korea MFDS, CDSCO and others.
With ‘Science for Life’ as our guiding principle, we’ve made a conscious choice to focus on what truly matters: advancing human and animal health, saving lives, and improving quality of life through meaningful science. Our work is grounded in public health, therapeutic innovation, and evidence-based safety.
Support the development of life saving medicines for humans and animals.
Ensure safety and biocompatibility in tools that extend and improve lives.
Ensure their safe use handling, and regulatory compliance and minimizing risk to human health.
We support your journey to develop new physical, chemical and biological products that enhance the quality of human life. We collaborate with you to ensure that your products are safe to use and compliant to the regulatory parameters through rigorous testing.
Conduct acute, sub-chronic, and chronic toxicity assessments in compliance with international guidelines.
Evaluate compounds and materials for effects on living systems to ensure regulatory compliance.
Provide sterility, microbial limit, and contamination testing to ensure product safety.
Evaluate medical devices as per ISO 10993 standards for global regulatory submissions.
Offer in vivo and in vitro models for CNS, respiratory, gastrointestinal, and other systems. Pharmacopeia-based tests, drug kinetics, pharmacodynamic studies.
Perform method development, validation, and stability studies for various compounds.
Every dataset we generate is fully traceable, reviewable, and backed by internal QA audits, ensuring regulatory readiness.
From raw data to final reports, our documentation is structured, comprehensive, and compliant with international standards.
Clients receive regular updates, real-time insights, and access to data during all phases of the study.
