Preclinical toxicology designed for IND approval
We expertly coordinate GLP-compliant toxicology studies with thoroughly vetted laboratories, ensuring that the data aligns perfectly with your clinical plan and regulatory agencies.
Acute, subchronic, chronic toxicity
Design and execution of short- and long-term toxicity studies, aligned with ICH guidelines and your clinical development timeline.
Reproductive and DART studies
Reproductive and developmental toxicity (DART) programs tailored to your compound class and trial strategy — from study design to reporting.
Safety pharmacology
Specialized studies to assess off-target effects and support safe first-in-human trials, using validated models and platforms.
Genotoxicity
Rapid turnaround genotox packages using GLP-validated assays — critical for small molecules and early IND submissions.
Why work with Davos
Preclinical execution with IND in mind.
CROs matched to your study needs
We select toxicology labs based on therapeutic area, compound type, and historical performance — not just availability.
Oversight from start to finish
With unified coordination of timelines, test article delivery, and formulation, we minimize risk and prevent surprises.
Strategy that starts with the end in mind
Every toxicology study we coordinate aligns with your IND timeline, regulatory goals, and overall development plan.
Execution you can trust in IND toxicology studies
Toxicology is high-stakes and time-sensitive. These numbers reflect the value of choosing the right lab — and the right coordinator.
With our expertise, oversight, and trusted partners, we deliver accelerated timelines with seamless execution.
Talk to a regulatory-aligned Toxicology expert
From GLP compliance to submission strategy — we help you get it right the first time.
Explore our Case Studies
Real-world applications of our services
FAQ's
Find answers to common questions about our pharmaceutical services and solutions.
DavosPharma is a leading provider of pharmaceutical services. We specialize in drug development outsourcing. Our goal is to streamline your drug development process.
Our Integrated IND Platform brings together global CDMOs, CROs, and expert consultants to manage every step — from CMC, toxicology, to regulatory filing — so you can open an IND faster with less overhead.
We offer a range of services including Discovery, Biologics, Small Molecule, Drug Product, and Toxicology. Each service is designed to meet the unique needs of our clients. Our expertise ensures high-quality outcomes.
Vendor matchmaking connects you with the right partner for your project. We align your budget, technical needs, and goals with our global network of vetted vendors — optimizing efficiency and maximizing the likelihood of success.
You can reach us through our Contact page. Fill out the lead form, and we will get back to you promptly. We look forward to discussing your needs.
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