General Toxicology Testing
Repeated Dose Studies are a cornerstone of preclinical safety assessment. At Vivotecnia, we offer GLP-compliant subacute, subchronic and chronic toxicity studies to evaluate the effects of repeated exposure to a test item over time. These studies are essential to determine the No Observed Adverse Effect Level (NOAEL) and are required for regulatory submissions across pharmaceutical, chemical, cosmetic and food sectors.
Preclinical regulatory CRO
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Repeated dose toxicity studies provide a detailed picture of how a compound behaves in the body under continuous exposure. They help to identify the evolution of potential systemic toxicity, support NOAEL determination, identification of dose-response relationships, histophysiological analysis of key organs and are mandatory for most regulatory toxicology packages.
Chemical
Food
Vivotecnia has a highly specialized bioanalytical unit that combines state-of-the-art technology with a multidisciplinary team of experts in regulated preclinical studies.
We have conducted hundreds of DRF and MTD studies to support toxicology packages for pharmaceutical, chemical, cosmetic and food industry clients.
Even for non-GLP studies, our infrastructure ensures full environmental control and traceability.
Our DMF/MTD studies are seamlessly integrated with GLP-compliant studies, reducing time and optimizing resources.
We apply the 3Rs to minimize animal use while ensuring robust and informative study designs.
Need to assess the long-term safety of
your compound? Let our team design and
conduct. Fully compliant repeated dose
study for your next development
milestone.
