The requirement was to reduce the use of external providers, taking advantage of the expertise available following the addition of the analytical team at the Labcorp Early Development Research Labs location in Eye, U.K.
Planning and managing any toxicology study can be a daunting prospect for anyone, particularly for inhalation studies, which present their own unique challenges.
As a leader in new approach methods (NAMs), Labcorp provides a range of non-animal test methods to evaluate inhalation toxicity during early development. With experience performing hundreds of assays each year, our dedicated in vitro toxicology team can design customized studies to meet your specific regulatory and scientific goals.
Cytotoxicity testing is a critical step in medical device evaluation, but it comes with many challenges. Factors like device composition, sample preparation and contamination can impact results. With so much riding on safety data, it's essential to understand these challenges.
SOT 2024 -- Acetone and ethanol are widely used in industrial processes and are found in common household products. In inhalation studies, these organic molecules are used as solvents to vaporize low-volatility chemicals to reach the target aerosol concentrations.
SOT 2024 -- The U.S. EPA OPPTS 870.6300 Test Guideline (TG), the OECD 426 TG and potential additions to OECD 443 study designs call for test batteries for assessing learning and memory (L&M) function in rodents around the time of weaning and at adulthood.
SOT 2024 -- The rat is a commonly used animal model for preclinical continuous intravenous infusion. Many continuous intravenous infusion models have been developed. Due to the possible irritant properties of some test articles, the favoured catherisation site has become the femoral vein.
SOT 2024 -- Developmental neurotoxicity (DNT) studies are a regulatory requirement for the testing of chemicals that may cause adverse neurodevelopmental outcomes.
SOT 2024 -- The purpose of this study was to define an approach within risk management to determine acceptable safety limits of an ultrasound gel for invasive applications based on the results of a systemic toxicity study using a wide range of concentrations of the gel.
