Expert pharmaceutical solutions
Whether you're identifiying a lead or considering a 2nd commercial vendor, we can help you move faster and with less risk.
Discovery services that set you up for IND Success
Hit-to-lead, ADME/PK, and early biology studies run through trusted, fast-moving CROs — aligned with your IND goals.
Downstream thinking
We design studies with your future filing in mind.
Quick CRO onboarding
Avoid long RFP cycles by working with groups we already know and trust.
Expert support for small molecule development
Scale up complex chemistry with fewer delays — from peptides and HPAPIs to halogenated APIs and controlled substances.
Specialized CDMO match
We know who can handle your chemistry safely and at scale.
Regulatory alignment
Ensure CMC, formulation, and documentation support your IND plan.
Biologics development with modality-matched partners
Get matched with CDMOs who have real experience with your modality — including antibodies, gene therapies, and RNA-based platforms.
No modality mismatch
We only recommend partners who’ve delivered similar biologics before.
Audit-ready facilities
Work with GMP vendors we’ve already vetted across North America, Europe, and Asia.
Comprehensive drug product development solutions
Build formulations that are manufacturable, scalable, and validated — from capsules to injectables.
Full formulation to fill-finish
We coordinate continuity between design, tech transfer, and packaging.
Custom excipients, real expertise
Tap into specialists in lipid systems, polymers, and advanced formats.
Toxicology programs designed for IND or NDA approval
Toxicology studies at vetted GLP labs - fully managed and aligned with regulatory expectations.
Right study, right species
We recommend the appropriate tox package based on your compound.
Oversight
We track shipments, study execution, and timelines — so you don't have to.
Not sure which service fits your program?
Tell us where you are in your development — we'll help map out the next steps and coordinate the right support.
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.
Still have questions?
We're here to help you with any inquiries.