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
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Bernadette M. Ryan, Ph.D., D.A.B.T. — Study Director
- Over 25 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
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Anne E. Doyle, Ph.D. — Study Director
- Over 8 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
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John C. Findlay, B.S. — Study Director
- Over 35 years of experience in toxicology
- Conducted more than 3000 GLP-compliant, pre-clinical toxicology studies
- Extensive background in rabbit and rat teratology studies, reproductive toxicology assessments
and neurotoxicity screening (FOB, delayed peripheral neuropathy and NTE assay)
- Managed NCI/NIH and NTP/NIEHS projects
- History of satisfying Sponsor expectations through careful planning, conducting and
supervising toxicology assessments
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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
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Michael Pendleton, B.S. — Study Director/Analytical Chemistry
- Over 25 years experience in analytical chemistry (GC, GC/MS, HPLC, ICP, FTIR, UV, etc.)
including methods development and validation
- Background includes experience supervising analytical laboratories; preparation and
analysis of dosing formulations (solutions, suspensions, injectables, etc.); homogeneity and stability
determinations
- Developed, implemented and maintained computer networks and LIMS
- History of interfacing computers and laboratory equipment and working with IT personnel
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Greg Ames, B.S.--Study Director/Pharmacokineticist
- Over 25 years of experience in pharmacokinetics
- Served as study director for assigned Pharmacokinetic, Toxicokinetic and ADME studies
- Performed pharmacokinetic calculations and interpreted results for TK and PK studies
- Designed, conducted and interpreted results for Radiolabeled (14C, 3H and 35S) ADME studies
in animals
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