| Karl A. Traul, Ph.D. | |
| | | |
| Expert Toxicology Consultant / Toxicologist |
| | - General Toxicology
- IND Product Safety Assessment and Documentation Preparation
- OEL Monographs
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| Areas of Toxicology Expertise: |
| | - Regulatory Toxicology-Safety Strategy and Documentation for Product Registration (e.g. FDA/EPA, JECFA, EU)
- Strength in Genetic, in Vitro Toxicology
- Developmental & Reproduction Toxicology Assessments
- OEL/Worker Safety Assessment Monographs
- Management of GLP Product Safety Studies
- Veterinary Drug/Additives
- GLP QA Evaluation GLP Archives/Document Security Center
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| Description: |
| | Ingle & Traul Pharmaceut. Consult. (6 years); American Cyanamid (9 years)-Associate Director of Toxicology, Director of Regulatory Compliance; Exxon Biomedical Sciences, Inc. (6.5 years)-Manager, Genetic & Reproductive Toxicology; Pfizer (11 years)-Product Safety Evaluation; SOT/MASOT, SQA, Genetic Toxicology Association, 68+ Publications. |
| Contact information |
| | Karl A. Traul, Ph.D. K.A. Traul Pharmaceutical Consulting 65 South Main Street - Bldg B Pennington, New Jersey 8534 Phone: (609) 818-1177 Fax: (609) 818-0999 Email: katraul (at) aol.com Website: http://rtctox.com/traul.htm | |
| Litigation Expert Witness: |
| | Willing to serve as Expert Witness | |
| | Experience as Expert Witness | |
| | |
| Dictionary of Abbreviations and Acronyms used: |
| Epa | Environmental Protection Agency |
| Eu | European Union |
| Fda | Food and Drug Administration |
| Glp | Good Laboratory Procedure |
| Glp Qa | Good Laboratory Procedure Qualtiy Assurance |
| Ind | Investigational New Drug |
| Jecfa | Joint FAO/WHO Expert Committee on Food Additives |
| Oel | Occupational Exposure Limits |
| Sot/Masot | Society of Toxicology/Mid-Atlantic Regional Chapter, Society of Toxicology |
| Sqa | Society of Quality Assurance |