Vivotecnia Research S.L
Vivotecnia is a leading independent European contract research organization (CRO) specializing in toxicology safety and preclinical studies. With over 20 years of experience, state-of-the-art GLP-accredited facilities, and a commitment to animal welfare and regulatory compliance, Vivotecnia supports pharmaceutical, biotech, chemical, cosmetic, agrochemical, and food industries worldwide. The company offers comprehensive services including safety studies, toxicology testing, advanced therapy development, and regulatory support, aiming to accelerate product development and ensure safety and efficacy.
Industries
Nr. of Employees
medium (51-250)
Vivotecnia Research S.L
Services
Full-service GLP study planning and execution to generate regulatory safety data for pharmaceuticals, chemicals, biocides, cosmetics and medical devices.
Acute, subacute, subchronic and chronic toxicology studies and in vitro assays (including NAMs) across multiple species and routes of administration.
Combined battery of in vivo acute toxicity tests (oral, dermal, inhalation) and in vitro irritation/sensitization assays to meet regulatory acute hazard information needs.
Acute and subchronic inhalation studies using flow-through chambers, multiple sampling points and gravimetric/analytical monitoring for vapors, aerosols and dust.
Short- and long-term ecotoxicity tests, biodegradability, fate and behavior studies and other Annex VII–X style programs to support regulatory dossiers.
Regulatory genotoxicity assay packages including bacterial reverse mutation (Ames), in vitro mammalian cell assays and in vivo follow-ups as required.
Full-service GLP study planning and execution to generate regulatory safety data for pharmaceuticals, chemicals, biocides, cosmetics and medical devices.
Acute, subacute, subchronic and chronic toxicology studies and in vitro assays (including NAMs) across multiple species and routes of administration.
Combined battery of in vivo acute toxicity tests (oral, dermal, inhalation) and in vitro irritation/sensitization assays to meet regulatory acute hazard information needs.
Acute and subchronic inhalation studies using flow-through chambers, multiple sampling points and gravimetric/analytical monitoring for vapors, aerosols and dust.
Short- and long-term ecotoxicity tests, biodegradability, fate and behavior studies and other Annex VII–X style programs to support regulatory dossiers.
Regulatory genotoxicity assay packages including bacterial reverse mutation (Ames), in vitro mammalian cell assays and in vivo follow-ups as required.
Expertise Areas
- Preclinical toxicology
- Regulatory compliance and GLP
- Inhalation toxicology
- Ecotoxicology and REACH registration support
Key Technologies
- Liquid chromatography (LC-UV/DAD)
- Gas chromatography (GC-FID/ECD)
- Gravimetric aerosol monitoring
- Flow-through inhalation exposure chambers