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| John M. Davitt, M.Sc. | ||
| Expert Toxicology Consultant / Toxicologist | ||
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| Areas of Toxicology Expertise: | ||
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| Description: | ||
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Regulatory experience includes 27 years
at FDA (Supervisory Pharmacologist / review and evaluation of
Human Drugs) and 14 years as a Pharmaceutical Regulatory
Consultant
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| Contact information | ||
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John M. Davitt 703
Midland Road
e-mail:
jdavitt.ras (at) verizon.net |
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| Forensic Expert Witness: | ||
| Willing to serve as Expert Witness | ||
| Experience as Expert Witness | ||
| Dictionary of Abbreviations and Acronyms used: | ||
| Dmf | Drug Master File | |
| Fda | Food and Drug Administration | |
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Ind |
Investigational New Drug | |
| Nda | New Drug Application | |
John Davitt Regulatory Pharmacology & Toxicology FDA veteran Ind Nda & Dmf
Regulatory Pharmacology & Toxicology Areas Toxicology Expertise: Pharmaceuticals
New Drug Evaluation Drug Safety Assessment Anti-infective Agents Dermatological
and Ophthalmologic Drugs
Ind, Nda & Dmf Submissions.
27 years at FDA (Supervisory Pharmacologist) - Directed and Participated in the
Review and Evaluation of Drugs Intended for Human Use