More than 15 years experience generating GLP toxicologic pathology reports. At Tox Path LLC we can perform the complex microscopic evaluation and interpretation of tissue sections from animals exposed to test materials and correlate these findings with necropsy, organ weight, and clinical pathology findings.Areas of expertise include authoring comprehensive GLP-compliant pathology narrative reports of microscopic, gross, and clinical pathology findings for IND purposes.Regularly peer reviewed by pathologists from many major pharmaceutical companies with which I have built a reputation of quality reporting and timeliness and developed positive professional relationships.Conduct formal peer reviews as needed.Communicate the significance of pathologic findings to study directors, clients and other individuals.Attend necropsies as required, and provide scientific guidance to necropsy technicians to ensure accuracy and compliance with protocols and SOP's.Interact with pathologists, necropsy technicians, histotechnologists, study directors, study coordinators, toxicologists and report coordination personnel.Provide scientific advice in evaluating current technical procedures and in the development of new procedures/techniques, including immunohistochemistry.Study activities can be conducted in accordance with the US-FDA Good Laboratory Practices (GLP) regulation (21 CFR Part 58) and OECD principles of Good Laboratory Practice (as revised in 1997), ENV/MC/CHEM(98) 17.