|
| John M. Davitt, M.Sc. | ||
| Expert Toxicology Consultant / Toxicologist | ||
| ||
| Areas of Toxicology Expertise: | ||
| ||
| Description: | ||
| Regulatory experience includes 27 years at FDA (Supervisory Pharmacologist / review and evaluation of Human Drugs) and 14 years as a Pharmaceutical Regulatory Consultant
| ||
| Contact information | ||
John M. Davitt 703 Midland Road e-mail: jdavitt.ras (at) verizon.net | ||
| 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 | |
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