Greenfield Pathology Services, Inc.
GPS
Your Guidance in the World of Toxicologic Pathology
Our Staff
Ken Schafer, DVM, PhD, Diplomate, ACVP, Fellow, IATP
Ken Schafer, DVM, PhD, Diplomate, ACVP, Fellow, IATP
Ken Schafer, DVM, PhD, Diplomate, ACVP, Fellow, IATP
Dr. Schafer founded Greenfield Pathology Services in 2019 and has over 20 years of experience working for pharmaceutical companies and a CRO. He brings integrity and depth of knowledge to the field of toxicologic pathology in his support of clients.
William (Bill) Jordan, DVM, PhD, Diplomate, ACVP
Ken Schafer, DVM, PhD, Diplomate, ACVP, Fellow, IATP
Ken Schafer, DVM, PhD, Diplomate, ACVP, Fellow, IATP
Dr. Jordan has over 30 years of experience in toxicologic pathology, having worked in both the pharmaceutical company and CRO arenas. Dr. Jordan leverages his extensive background in neuropathology and general toxicologic pathology in support of clients pursuing drug development.
Dennis Hoover, DVM, PhD, Diplomate, ACVP
Ken Schafer, DVM, PhD, Diplomate, ACVP, Fellow, IATP
Frances Clemo, DVM, PhD, Diplomate, ACVP (Clinical and Anatomic)
Dr. Hoover has extensive experience in toxicologic pathology, having led the pathology department in a large pharmaceutical company. Dr. Hoover brings this broad base of experience to GPS in primary pathology evaluations and peer review.
Frances Clemo, DVM, PhD, Diplomate, ACVP (Clinical and Anatomic)
Frances Clemo, DVM, PhD, Diplomate, ACVP (Clinical and Anatomic)
Frances Clemo, DVM, PhD, Diplomate, ACVP (Clinical and Anatomic)
Dr. Clemo has over 20 years of experience in toxicologic pathology (clinical and anatomic pathology), having worked in various pharmaceutical and CRO companies. Dr. Clemo will support clients through her in-depth clinical pathology knowledge of many small molecule, medical device, and biotherapeutics programs.
Suzanne Neu, DVM, PhD, Diplomate, ACVP
Frances Clemo, DVM, PhD, Diplomate, ACVP (Clinical and Anatomic)
Julie Hutt, DVM, PhD, Diplomate, ACVP
Dr. Neu has over 25 years of toxicologic pathology experience in pharmaceutical company and CRO environments, plus 10 years of experience in diagnostic pathology. She has experience with a variety of species beyond the usual laboratory animals including livestock such as cattle, horses, pigs, and sheep.
Julie Hutt, DVM, PhD, Diplomate, ACVP
Frances Clemo, DVM, PhD, Diplomate, ACVP (Clinical and Anatomic)
Julie Hutt, DVM, PhD, Diplomate, ACVP
Dr. Hutt has nearly 20 years of toxicologic and investigative pathology experience, having worked previously at CROs and an inhalation toxicology research institute. She has experience in target animal species studies using cattle, horses, pigs and poultry. She uses her background in general and inhalation toxicologic pathology to suppor
Dr. Hutt has nearly 20 years of toxicologic and investigative pathology experience, having worked previously at CROs and an inhalation toxicology research institute. She has experience in target animal species studies using cattle, horses, pigs and poultry. She uses her background in general and inhalation toxicologic pathology to support clients in the development of small molecule and biotherapeutics programs.
Brad Njaa, BSc, DVM, MVSc, Diplomate, ACVP
Deepa B. Rao, BVSc, MS, PhD, Diplomate, ABT, Diplomate, ACVP, Fellow, IATP
Greg Hall, DVM, PhD, Diplomate, ACVP
Dr. Njaa supports GPS with otic pathology assessments. Dr. Njaa has had a long standing interest in the ear, having published book chapters on the pathology of the ear and clinical investigations of otic pathology.
Greg Hall, DVM, PhD, Diplomate, ACVP
Deepa B. Rao, BVSc, MS, PhD, Diplomate, ABT, Diplomate, ACVP, Fellow, IATP
Greg Hall, DVM, PhD, Diplomate, ACVP
Dr. Hall has extensive experience in neuropathology assessment in nonclinical toxicology studies. Greg brings to GPS over 20 years of experience supporting drug development in a large biopharma setting with a focus on neurology indications.
Deepa B. Rao, BVSc, MS, PhD, Diplomate, ABT, Diplomate, ACVP, Fellow, IATP
Deepa B. Rao, BVSc, MS, PhD, Diplomate, ABT, Diplomate, ACVP, Fellow, IATP
Deepa B. Rao, BVSc, MS, PhD, Diplomate, ABT, Diplomate, ACVP, Fellow, IATP
Dr. Rao is a board-certified toxicologist and veterinary toxicologic pathologist with over 20 years of experience in the translation of chemical/drug toxicological data from animal studies to human health risk assessment. Her specialized expertise is in regulatory neurotoxicology and neuropathology.
Cindy Farman, DVM, PhD, Diplomate, ACVP
Shelley L. Patrick, DVM, Diplomate, ACVP
Deepa B. Rao, BVSc, MS, PhD, Diplomate, ABT, Diplomate, ACVP, Fellow, IATP
Dr. Farman has over 20 years of experience in toxicologic pathology, including at CROs, biotechnology companies, and as a pathology consultant. She has extensive experience in ocular pathology, including serving as the pathologist providing support and scientific expertise to an entire ocular therapeutic platform at a large biotechnology company.
Shelley L. Patrick, DVM, Diplomate, ACVP
Shelley L. Patrick, DVM, Diplomate, ACVP
Shelley L. Patrick, DVM, Diplomate, ACVP
Dr. Patrick has nearly 20 years of experience as a toxicologic pathologist at two large CROs. She has vast experience serving as a study pathologist supporting clients from biotech, chemical,and pharmaceutical organizations. In addition to her general toxicologic pathology expertise, she has special interest in neuropathology and carcinogenicity studies.
James Reindel, DVM, PhD, Diplomate, ACVP
Shelley L. Patrick, DVM, Diplomate, ACVP
Shelley L. Patrick, DVM, Diplomate, ACVP
Dr Reindel comes to GPS with over 30 years of toxicologic pathology experience with large pharma, biotech, and CRO organizations. He has been intimately involved in leadership and has significant experience in product development. He has expertise in primate pathology and a broad range therapeutic areas (CNS, inflammation, immunology, o
Dr Reindel comes to GPS with over 30 years of toxicologic pathology experience with large pharma, biotech, and CRO organizations. He has been intimately involved in leadership and has significant experience in product development. He has expertise in primate pathology and a broad range therapeutic areas (CNS, inflammation, immunology, oncology) and treatment modalities including small molecule and biotech products.
James T. Meehan, DVM, PhD, Diplomate, ACVP
James T. Meehan, DVM, PhD, Diplomate, ACVP
James T. Meehan, DVM, PhD, Diplomate, ACVP
As a toxicologic pathologist for nearly 30 years at major CROs and a large pharmaceutical company, Dr. Meehan recognizes that a CRO can provide a client not only additional capacity but critical experience and expertise. Jim has had an emphasis in neurotoxicity and ultrastructural pathology that supplement his skills acquired from the evaluation of general and varied specialty toxicity studies.
Ms Wendy Rhoades
James T. Meehan, DVM, PhD, Diplomate, ACVP
James T. Meehan, DVM, PhD, Diplomate, ACVP
Wendy Rhoades is the contracts manager for GPS. Wendy has 20 years of experience in nonclinical research and development working for both CROs and Sponsor companies. Wendy brings her experience in contract management and negotiation, project management, and organizational leadership to the GPS team.
About Us
Experience
Experience
Experience
All of our pathology staff are experienced toxicologic pathologists with 20 or more years of experience each. This includes primary evaluation and peer review of all types of studies, from discovery and lead optimization to carcinogenicity assessment.
GPS
Experience
Experience
GPS: Your Guidance in the World of Regulated Toxicologic Pathology. We strive to help clients, including businesses large and small, with toxicologic pathology needs from slide evaluation to peer review to white papers and expert consulting to pathology working groups to advice on pathology in regulatory submissions.
Expertise
Experience
Expertise
Our pathologists bring added expertise to the table, beyond the evaluation of routine toxicology studies. This expertise is in the areas of ocular, otic, neuropathology, respiratory system, and carcinogenicity study assessment as well as extensive drug development experience.