Preclinical & Toxicological Services
(As per OECD, NDCT, ICH, MHRA, USFDA/EPA Guidelines)
  • Acute Toxicity Studies (Oral, Dermal, Inhalation and Parenteral)
  • Eye/ Skin Irritation Studies
  • Skin Sensitization Studies (GPMT/ Buehler)
  • Repeated Dose Toxicity Studies (Sub-acute, Sub-chronic and Chronic)
  • Carcinogenicity Studies
  • Neurotoxicity Studies
  • Reproduction and Developmental Toxicity Studies (DART)
  • Maximum Tolerated Dose (MTD) Studies
  • Dose Range Finding (DRF) Studies
  • In-vitro Toxicology Studies
  • Ecotoxicology Studies
  • Pharmacokinetic and Toxicokinetic Study of Pharma & Biosimilars
  • DMPK Study
  • Efficacy Study Models (Anti-Cancer, Anti-Diabetes, Xenograft, Psoriasis etc.)
  • PDE Studies (EMA/CHMP/ CVMP/ SWP/169430/2012)
  • In-Silico QSAR Studies (ICH M7)

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