Preclinical CRO Accelerating Drug and Device Development
Accelerate your preclinical research
We are an advanced preclinical CRO that provides comprehensive solutions across drug and device development phases. Our services include contract research and development, bioanalysis, analytical testing, pharmacodynamic modeling, preclinical safety testing, and more.
Preclinical CRO Accelerating Drug and Device Development
Accelerate your preclinical research
We are an advanced preclinincal CRO that provides advanced comprehensive solutions across drug and device development phases including bioanalysis, contract research and development, clinical CRO, advanced preclinical services, analytical testing, GLP lab, discovery and research, pharmacodynamic modeling, and preclininal safety testing.
Preclinical CRO Accelerating Drug and Device Development
Accelerate your preclinical research
We move in unison with you toward your goals with preclinical testing and bioanalytical expertise and services that deliver your drug to market faster. Uncover new opportunities that will impact and transform lives with Noble Life Sciences.
Advance your innovation. Reduce risk. Achieve compliance.
Comprehensive Preclinical CRO Services
Noble Life Sciences supports drug, biologic, cell and gene therapy, and medical device programs across the full preclinical lifecycle. From early discovery through IND enabling and GLP toxicology, our teams deliver scientifically rigorous studies designed to meet regulatory expectations.
Advance your innovation. Reduce risk. Achieve compliance.
Comprehensive Preclinical CRO Services
Noble Life Sciences supports drug, biologic, cell and gene therapy, and medical device programs across the full preclinical lifecycle. From early discovery through IND enabling and GLP toxicology, our teams deliver scientifically rigorous studies designed to meet regulatory expectations.
Advance your innovation. Reduce risk. Achieve compliance.
Comprehensive Preclinical CRO Services
Noble Life Sciences supports drug, biologic, cell and gene therapy, and medical device programs across the full preclinical lifecycle. From early discovery through IND enabling and GLP toxicology, our teams deliver scientifically rigorous studies designed to meet regulatory expectations.
Therapeutic Areas
In vivo and in vitro preclinical models supporting oncology and infectious disease research, pharmacodynamic studies, and translational development for small molecules and biologics. Accelerate your path to market with expert preclinical research designed to reduce risk and generate decision ready data.
Oncology
As an oncology contract research organization, our preclinical oncology and immuno-oncology services include cancer preclinical animal model testing, in vivo cancer models, OncoDiversity Cell Line Panel, and Pharmacodynamic Models.
Infectious Diseases
Our infectious disease services include SARS-CoV-2 research solutions, antiviral testing labs, and vaccine research for influenza and RSV drug development. We also offer antiviral, antibacterial drug and vaccine discovery and development for a multitude of viral and bacterial pathogens that lead to sepsis.
Diabetes
Reliable experts will conduct your preclinical diabetes studies using a variety of different models to determine the safety and efficacy of your therapeutics.
World-class scientists. Groundbreaking technology.
Cell & Gene Therapy
World-class scientists. Groundbreaking technology.
Cell & Gene Therapy
From the early stages of cell and gene therapy development, our goal is to make your transition from to commercialization as seamless as possible. We are dedicated to delivering the highest quality cell and gene development services.
World-class scientists. Groundbreaking technology.
Cell & Gene Therapy
Medical Devices
Get your device to market faster and uncover new opportunities to impact people’s lives with our research expertise.
A preclinical contract research organization to accelerate your GLP preclinical study and Non-GLP preclinical research services for IND filing.
Facilities & Compliance
Learn about our state-of-the-art facility with a commitment to compliance.
Facilities
Noble has FDA inspected GLP facilities, is accredited by AAALAC, and operates in full accordance with the Animal Welfare Act.
Compliance
We maintain the highest GLP standards and deliver the necessary research data required to achieve FDA compliance.





