Liveon Biolabs Toxicology
Read More


At Liveon Biolabs, we understand the importance of toxicology data for regulatory approvals. Our expert toxicologists provide below toxicology studies as per OECD, US FDA, ISO and Schedule Y guidelines.

In Vivo Toxicology Studies

  • Maximum Tolerable Dose(MTD)
  • Dose Range Finding (DRF)
  • Acute Toxicity studies
  • Sub-acute Toxicity Studies (14 and 28 days)
  • Sub-Chronic and Chronic Toxicity Studies
  • Skin, Mucous Membrane and Eye Irritation Studies
  • Skin Sensitization Studies (GPMT)
  • Immunogenicity Studies
  • Local Lymph Node Assay (LLNA) by BrdU ELISA
  • Reproductive and Developmental Toxicology Studies
  • Carcinogenicity studies
  • Uterotrophic and Hershberger assays for endocrine disruption

Genetic Toxicology Studies

  • Bacterial Reverse Mutation Test (Ames test)
  • In vitro Mammalian Chromosome Aberration Test
  • In vitro Micronucleus Test
  • In vivo Mammalian Erythrocyte Micronucleus Test
  • In vivo Mammalian Bone Marrow Chromosome Aberration Test
  • Cell Gene Mutation

In Vitro Services

  • Cytotoxicity
  • MTT Assay

Alternative to Animals Models

  • In Vitro Skin Irritations/Corrosion
  • Hen’s Egg Test – Chorioallantoic Membrane (HET-CAM)
  • In Vitro Skin/Dermal absorption using Ex vivo skin models

Route of Administration

Liveon Biolabs has expertised in below routes of administrations for in vivo studies :

  • Oral (PO)
  • Intravenous (IV)
  • Intradermal(ID)
  • Intraperitoneal (IP)
  • Subcutaneous (SC)
  • Intramuscular (IM)
  • Topical
  • Ocular, Intraocular, Intravitreal and Intracorneal
  • Intratracheal
  • Sublingual in Rabbits