iuvo brings decades of experience in preclinical development of pharmaceutical compounds to assist your team in developing new therapies. Our experienced consulting team can help you develop strategies and protocols, and our in-house testing facilities are at your disposal to execute the critical studies you need to move your program forward.
From early research, pharmacokinetics, and dose ranging studies to your definitive GLP studies, we can work with you to meet both your needs and relevant regulatory standards. We also provide custom-designed protocols and can work side-by-side with your scientists in our facility when the study design dictates your direct hands-on involvement.
Our species models include mice, rats, guinea pigs, hamsters, and rabbits. Our expert in vivo team can dose by a variety of routes including, but not limited to, po, iv, ip, sc, im, dermal, intratracheal, ocular/intraocular, intranasal, rectal, and intravaginal.
To contact our specialists or learn more about our services, please reach out to us, and we’d be happy to help you with your application.
- Analytical Method Development and Validation Testing
- Antimicrobial Effectiveness Testing
- Bacterial Endotoxin Testing
- Bioburden Testing
- Biologics Safety Testing
- Biologics Testing Services
- Cytotoxicity Testing
- D Value / Population Testing
- Environmental Monitoring and Assessment Testing
- Extractables and Leachables Testing
- General Toxicology Testing Services
- Genetic Toxicology Testing
- Heterotrophic Plate Count Testing
- Microbial Limits Testing
- Ophthalmic – Pharmaceuticals Testing
- Package Integrity Testing
- Sensitization Testing
- Stability Studies Testing
- Sterility Testing
