Enhancing Drug Development with Virscio’s GLP Toxicology Services
Virscio: Your Trusted Partner in GLP Compliant Toxicology Research
Virscio's GLP Toxicology Services provide clarity and confidence from preclinical proof-of-concept to IND-enabling studies, improving the odds of clinical translation. With over 20 years of experience in preclinical research, Virscio integrates advanced methodologies and validated nonhuman primate models, prioritizing animal welfare and robust quality systems. Our approach is designed to reduce the time, cost, and risk associated with therapeutic development across various medical fields.
In this overview, we examine how Virscio serves a trusted partner for GLP in vivo toxicology research. Our services support critical development stages, encompassing preclinical strategy, protocol design, study execution, data analysis, and regulatory path definition, with a special focus on preclinical histology, tissue pharmacodynamics, and in vivo primate delivery pharmacokinetics, pharmacodynamics, efficacy, and safety.
Learn how Virscio’s GLP Toxicology Services can support your research, offering a comprehensive range of capabilities for effective and efficient drug development.
Discover Our Toxicology Services Now!
Learn how Virscio’s GLP Toxicology Services can support your research, offering a comprehensive range of capabilities for effective and efficient drug development.
Virscio's extensive scientific and technical expertise spans disease modeling, pharmacodynamics, pharmacokinetics, and toxicology, ensuring comprehensive service provision from initial study design to execution and reporting.
In this overview of our GLP Toxicology Services, you will learn about:
- Virscio's commitment to de-risking innovation and providing world-class research capabilities across various preclinical disciplines.
- The range of GLP and non-GLP capabilities offered, including delivery and distribution, pharmacokinetics and pharmacodynamics, efficacy, and exploratory safety and toxicology.
- Our unparalleled access to biologically clean primates, allowing for timely initiation of studies tailored to specific research objectives.
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