In Vivo REACH Services
Performing testing when in vitro studies cannot be used to predict biological responses
This includes: OECD 402: Acute Dermal Toxicity, OECD 403: Acute Inhalation Toxicity, OECD 404: Acute Dermal Irritation/Corrosion, OECD 405: Acute Eye Irritation/Corrosion, OECD 406: Skin Sensitisation, OECD 407: Repeated Dose 28-day Oral Toxicity Study in Rodents, OECD 408: Repeated Dose 90-Day Oral Toxicity Study in Rodents, OECD 410: Repeated Dose Dermal Toxicity: 21/28-day Study, OECD 411: Subchronic Dermal Toxicity: 90-day Study, OECD 412: Subacute Inhalation Toxicity: 28-Day Study, OECD 413: Subchronic Inhalation Toxicity: 90-day Study, OECD 414: Prenatal Developmental Toxicity Study, OECD 416: Two-Generation Reproduction Toxicity, OECD 420: Acute Oral Toxicity - Fixed Dose Procedure, OECD 421: Reproduction/Developmental Toxicity Screening Test, OECD 422: Combined Repeated Dose Toxicity Study with the Reproduction/Developmental Toxicity Screening Test, OECD 423: Acute Oral toxicity - Acute Toxic Class Method, OECD 425: Acute Oral Toxicity: Up-and-Down Procedure, OECD 426: Developmental Neurotoxicity Study, OECD 436: Acute Inhalation Toxicity – Acute Toxic Class Method, OECD 451: Carcinogenicity Studies, OECD 452: Chronic Toxicity Studies, OECD 474: Mammalian Erythrocyte Micronucleus Test, OECD 475: Mammalian Bone Marrow Chromosomal Aberration Test, OECD 486: Unscheduled DNA Synthesis (UDS) Test with Mammalian Liver Cells in vivo
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