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. Read More

Department of Scientific & Industrial Research (DSIR)

OECD Good Laboratory Practice (GLP) Certification

Central Drugs Standard Control Organisation (CDSCO)

Drugs Control Department Government of Karnataka

ISO 9001:2008 Quality Management System

Institutional Animal Ethics Committee (IAEC)

National Accreditation Board for Testing and Calibration Laboratories (NABL)
Reliability
You can Audit
Every dataset we generate is fully traceable, reviewable, and backed by internal QA audits, ensuring regulatory readiness.
Documentation
that withstands
scrutiny
From raw data to final reports, our documentation is structured, comprehensive, and compliant with international standards
Transparency at
every stage
From raw data to final reports, our documentation is structured, comprehensive, and compliant with international standards
46 & 47, Water Tank Rd, 2nd Phase, KIADB Industrial Area, Antharasanahalli, Tumakuru – 572106, Karnataka, India.
+91 9480849732, 33
info@liveonbiolabs.com