Pathology Experts provides you with the highest level of independent expertise in toxicologic pathology and related translational research. Our focus is on maintaining a team of highly experienced pathologists supported by the latest data capture software, globally standardized SOP's and report formats, communications, stringent quality control requirements and customer support capabilities.
Pathology Experts is a center of expertise for interpretation and translation of data from biotherapeutic safety assessment studies, including monoclonal antibodies, recombinant proteins, RNA and gene therapy products. We understand the importance of determining the relevance of animal data, particularly immune reactions, to human safety.
Digital Pathology- Annotation and QC support for ML/DT algorithm development
Our expert level toxicologic pathologists provide domain expertise in all organ systems for QC, training and validation of Machine Learning/Deep Thinking algorithms for accurate and consistent evaluation of WSIs.
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How can we help you - examples:
- Expert histopathology evaluations
- External histopathology peer reviews
- Independent histopathology assessments
- Expert clinical pathology (hematology and clinical chemistry) evaluations
- External clinical pathology peer reviews and independent assessments
- Risk Management of in vivo study findings and nonclinical development safety issues
- Participation in sponsor advisory boards
Pathology Experts provides access to the comparative neurobiology and neuropathology knowledge and experience needed to address discovery and development questions of advanced cellular and gene therapies, biologics, medical devices, and small molecules needed to treat diseases of the nervous system.
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Our years of experience in the pharmaceuticals and biologics industry makes us ideal partners for addressing regulatory issues; preparation of regulatory documentation; appearances at regulatory agencies; expert report preparation; independent assessments and routine GLP-histopathology.
Read about recommended best practices for determining, communicating, and using adverse effect data from nonclinical studies in this paper.
Extend Your Resources
Pathology Experts can be your "Virtual Toxicologic Pathology Department". Providing your company with additional expertise, resources and flexibility to meet your timetable with world class subject matter experts in the preclinical phase of compound and device development.
Contact us regarding our options for providing preclinical services via individual or teams of Experts focussed on your compound or therapy. We can design a short or long term plan for a "virtual team" of experts that you can integrate into your development timetable and budget.