Our GLP-compliant pathology services support toxicology and biocompatibility studies through integrated histopathology, clinical pathology, and electron microscopy evaluations. Studies are conducted in accordance with OECD GLP principles and include comprehensive necropsy procedures, organ weight analysis, and advanced histotechnology processes such as tissue fixation, processing, microtomy, H&E staining, and specialized staining techniques. Histopathological assessments are performed by board-eligible and board-certified toxicologic pathologists using internationally recognized STP / INHAND nomenclature to ensure harmonized lesion interpretation and regulatory consistency.
In addition to microscopic pathology evaluations, we provide complete clinical pathology testing including haematology, coagulation, clinical chemistry, and urinalysis to support systemic toxicity assessments and safety evaluations. Our services also include local tissue reaction grading for implant studies in accordance with ISO 10993-6:2016 Annex E requirements. All pathology findings are supported by independent peer-reviewed reporting practices designed to deliver scientifically reliable, regulatory-ready data for pharmaceuticals, medical devices, chemicals, biomaterials, and other nonclinical safety studies.