General Toxicology
Taking a Drug to the market is a long and complex process that requires a knowledge intensive work and a multidisciplinary team. Vivotecnia's aim is to help you with the non-clinical research throughout the development of your product.
Vivotecnia offers regulatory-level toxicology studies conducted under GLP standards. Protocols are designed according to sponsor’s strategy for preclinical development and in compliance with guidelines issued by international regulatory bodies (EMEA, FDA, OCDE, ICH…). We take care of providing the non-clinical studies you require for the registration dossier of your product.
We offer a wide range of experimental models in toxicology in which we can perform repeated dose protocols through different routes and up to different durations.
Experimental models for repeated dose toxicity studies
| Species | Strain | duration |
| - Rat | (Wistar - SD...) | 6 months |
| - Mouse | (CD1 - Balb/c...) | 6 months |
| - Dog | (Beagle) | 3 months |
| - Rabbit | (New Zealand White) | 3 months |
| - Pig | (Gottingen mini-pig) | 6 months |
Administration routes
| - oral | - dermal | - ophthalmic |
| - inhalation | - intradermal | - intraperitoneal |
| - intramuscular | - intravenous | - subcutaneous |
Furthermore, we are aware of the importance of timings in a development program and thus give the highest importance to time optimization and meeting deadlines.