Experimur Toxicology Testing and Research
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Our Staff
Key Staff
Principals
Study Directors
Support Staff
STUDY DIRECTORS
Nabil Hatoum, Ph.D., D.A.B.T. Study Director
  • Over 30 years of experience in toxicology; last 27 in contract R&D
  • Skilled in the design and conduct of non-clinical and regulatory toxicology studies (FDA, EPA and OECD)
  • Extensive background in managing the technical and financial aspects of large programs, divisions and departments
  • History of maintaining close liaison and working relations with Sponsors
  • Diplomate of the American Board of Toxicology
Bernadette M. Ryan, Ph.D., D.A.B.T. Study Director
  • Over 29 years of "hands on" experience in toxicology
  • Conducted over 2500 GLP-compliant toxicology studies that ranged from chronics to acutes and included specialized evaluations and custom designs
  • Established institutional capabilities for developmental/reproductive and neurotoxicity evaluations and conducted numerous studies thereof
  • History of successful interactions with Sponsors QAUs, FDA and EPA auditors
  • Diplomate of the American Board of Toxicology
Anne E. Doyle, Ph.D., D.A.B.T. Study Director
  • Over 11 years of experience in academic and pre-clinical toxicology research
  • Key participant in the design and conduct of general toxicology as well as teratology, reproduction and neurotoxicity studies
  • Significantly contributed to the development of institutional capabilities in acoustical startle response and learning and memory paradigms for neurotoxicity
  • Extensive background in data analyses, interpretation and report writing
  • History of successful interaction with Sponsors, support laboratories and Experimur QA and technical staff
  • Diplomate of the American Board of Toxicology
John P. Devine, D.A.B.T. Study Director
  • Over 25 years of experience in pre-clinical toxicology testing and research
  • Key participant in the design and conduct of general toxicology, carcinogenicity and vaccine studies
  • Authored over 300 scientific reports, peer reviewed articles, and ADMET for Medicinal Chemists
  • Extensive background in data analyses, interpretation and report writing
  • History of successful interaction with Sponsors, support laboratories and regulatory auditors (FDA, EPA, and USDA)
  • Diplomate of the American Board of Toxicology
Bjorn A. Thorsrud, Ph.D. Study Director
  • Over 20 years of experience in preclinical toxicology
  • Extensive expertise in developmental and reproductive toxicology (DART) including infant nutrition
  • Familiar with pharmaceutical and chemical regulatory requirements
  • History of successful interactions with Sponsors, QA and regulatory auditors (FDA, EPA, USDA)
  • Past President of the Michigan Chapter of the Society of Toxicology
Edward J. Mallett, B.S. Study Director
  • Over 25 years of experience in toxicology
  • Conducted more than 2000 GLP-compliant, pre-clinical toxicology studies
  • Significantly contributed to the development of institutional capabilities of rat and rabbit teratology, sperm morphology, and FOB screen for neurotoxicity
  • Extensive background in supervising and conducting subchronic, chronic, teratology and reproduction studies
  • History of successful interaction with laboratory staff, report writers and QA personnel