Our Innovative Solutions
Our innovations continue to set the standard of excellence to meet global customer needs. Our products offer a major step up in terms of isolation, robustness and ease of use.
Our Services
Custom Made Products
Annual Maintenance Service
Design and Implementation
“Our vision is to combine our knowledge of shielding technology with our engineering skills to design, manufacture, install and commission shielding systems to the wireless enterprises.”
-Shivshankar
WHY CHOOSE LIVEON ?
We host an excellent Research and Development lab setup administered by highly competent engineers, technicians and staff who continually work to explore new innovations and stay up to date with the latest technologies in our space. Our lab is equipped with top-notch testing instruments to help our engineers maintain the highest level of integrity in RF Shielding, Testing and measuring standards.
TESTIMONIAL
ABOUT US
who you are and why they should choose your business.
Services
Latest News
- June 25, 2025 Liveon Biolabs Launches New Preclinical Research Facility
- June 15, 2025 Now Offering Advanced In-Vivo Toxicology Testing
- May 30, 2025 GLP Certification Successfully Renewed
- May 12, 2025 Animal Facility Now ISO Certified
Advancing global health through reliable preclinical research.
Trusted Partner for Regulatory-Compliant Safety and Efficacy Studies.
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 and 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, and add more details.
With ‘Science for Life’ as our guiding principle, we’ve made a consciouschoice 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.
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That’s why we specialize in regulatory testing for :
Pharmaceuticals and Biologics
supporting the development
of life saving medicines for humans and animals.
Medical Devices
ensuring safety and
biocompatibility in tools that extend and improve lives.
Agrochemicals and food safety
protecting ecosystems and food chains that ultimately impact human health.
Industrial Chemicals
ensuring their safe use, handling, and regulatory
compliance—minimizing risk to human health.
Our core services includes :
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.
Toxicology studies
Conducting acute, sub-chronic, and chronic toxicity assessments in compliance with international guidelines.
Pharmacology Models
Offering in vivo and in vitro models for CNS, respiratory, gastrointestinal, and other systems. Pharmacopeia based test, drug kinetics and drug pharmacodynamic studies.
Genotoxicity & Cytotoxicity
Evaluating compounds and materials for effects on living systems to ensure regulatory compliance.
Biocompatibility Testing
Evaluating medical devices as per ISO 10993 standards for global regulatory submissions.
Microbiology Services
Providing sterility, microbial limit, and contamination testing to ensure product safety.
Analytical Chemistry
Performing method development, validation, and stability studies for various compounds.
Accreditations and Compliance:
What are we know for :
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:
Clients receive regular updates, real-time insights, and access to data
during all phases of the study.
Conducting acute, sub-chronic, and chronic toxicity assessments in compliance with international guidelines..
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