Histopathology Services

GLP-certified histopathology complementing our preclinical bioanalysis services featuring our partner Patconsult.

Kymos Group’s strategic partner PATCONSULT provides GLP-certified histopathology evaluation and consultancy services in order to complement our preclinical bioanalytical offer.

Our full service includes sample processing, histopathologic diagnosis plus case-by-case pathology consultancy and targets preclinical and medical device developers in need of studies on preclinical regulatory, animal toxicology, tolerance, and experimental models.

Our histopathology team is fully equipped with a vacuum infiltration processor, workstation embedding center, Leica RM2255 Fully Automated Rotary Microtome, a Hamamatsu Digital Slide Scanner, and PathData histopathological data management system.

microbiological testing
Histopathology

Services

Histopathology Services

Histotechniques

  • Sample processing (microtomy, embedding, staining) with all usual pathology species.
  • Histological preparation of 50.000 – 70.000 organs/tissues per year.
  • Organ trimming according to RITA recommendations for GLP toxicity studies in rat.
  • Digital slide scanning.

  • GLP toxicologic pathology for preclinical regulatory studies.
  • Experimental pathology assays for new experimental models.
  • Biocompatibility and tolerance studies for medical devices in subcutis, muscle, and bone.

  • Design of preclinical/experimental pathology studies.
  • Specific histopathology problems.
  • Worldwide network of histopathology partners.

Services

Related services to Histopathology

Oligo testing

Bioanalysis of Nucleic Acids

Quantification of nucleic acids as therapeutics, biomarkers or similar with standardized and reproducible methods according to GLP.

Small molecules

Bioanalysis of Small Molecules & Generics

Development and validation of analytical methods for analysis of biological samples delivered mainly from pre-clinical and clinical studies.

LC-MSMS Sciex API 5500 QTrap

Bioequivalence Studies

Bioanalysis for bioequivalence studies of generics in collaboration with the sponsor and/or the selected clinical phase centre.

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