Earl Meierhenry work email
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Earl Meierhenry personal email
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I am a Veterinary Anatomic Pathologist with twenty-one years experience in the fields of toxicologic pathology, drug development, and safety studies, including eleven years with Roche Pharmaceuticals and 7 years with Charles River Laboratories. Forty scientific publications.Extensive interaction with study directors, senior management, and sponsors; and I would welcome the opportunity to share my expertise in drug development and safety studies. Histopathology, drug antibody conjugates, monoclonal antibodies, biosimilars, immunohistochemistry, tissue cross reactivity, digital pathology, necropsy supervision, histopathology peer review, and report evaluation.
Toxicologic Pathology Consulting And Development - Preclinical Development
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Toxicologic Pathology Consulting And Development - Preclinical DevelopmentCalifornia, United States
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Senior Veterinary Pathologist/CeoToxicologic Pathology Consulting And Development - Preclinical Development Dec 2016 - PresentTwenty-one years of experience in the pharmaceutical industry, preclinical development, and safety studies. Toxicologic pathologist for non-GLP and GLP preclinical studies in support of FDA and regulatory submissions. Excellent interpersonal skills for scientific interaction in study design and program development.Expertise in histopathology, drug antibody conjugates, monoclonal antibodies, immunohistochemistry, biosimilars, tissue cross reactivity, digital pathology, and necropsy supervision. Histopathology peer review and report evaluation. Special interest in non-human primate pathology. 40 scientific publications.
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Senior Veterinary PathologistCharles River Laboratories Jan 2010 - Dec 2016Wilmington, Massachusetts, UsPathologist on preclinical toxicology studies and project teams involving data evaluation and INDand NDA preparation for FDA submission.Study design, method development, and peer review.Digital pathology, drug antibody conjugates, monoclonal antibodies, biosimilars, immunopathology, and tissue cross-reactivity. -
Senior Veterinary PathologistRoche Pharmaceuticals 1998 - 2009Switzerland 🇨🇭 , ChPathologist on toxicology projects and planning teams in support of new drug development.Study director, CRO peer review, histopathology, genetically engineered mice, and hepatic and cardiacmodel development. Investigators Brochures for IND submission. -
Veterinary Pathologist/ToxicologistState Of California Dec 1990 - Feb 1998Designed and reviewed pathology and toxicology research submitted for pesticide registrations and biotechnology working groups. Provided recommendations concerning exposure hazards, risk assessment, and testing procedure to ensure compliance with adequate protocols, guidelines, and sound scientific practice. Toxicology Informatics.
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Senior Research AssociateWarner-Lambert/Parke Davis, Pharmaceutical Research Division Jul 1987 - Dec 1990Active in various aspects of drug development, including preclinical study director, Toxicologic pathology, carcinogenicity studies, planning teams, Good Laboratory Practices, and CRO peer review. Project Manager assignments included the effects of drug and nutrient interactions on toxicity and preclinical testing of anticonvulsant drugs.
Earl Meierhenry Skills
Earl Meierhenry Education Details
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University Of California, DavisComparative Pathology -
Kansas State UniversityDvm
Frequently Asked Questions about Earl Meierhenry
What company does Earl Meierhenry work for?
Earl Meierhenry works for Toxicologic Pathology Consulting And Development - Preclinical Development
What is Earl Meierhenry's role at the current company?
Earl Meierhenry's current role is Toxicologic Pathology and Preclinical Development 530-400-4712 earl.meierhenry@gmail.com.
What is Earl Meierhenry's email address?
Earl Meierhenry's email address is ea****@****ver.com
What schools did Earl Meierhenry attend?
Earl Meierhenry attended University Of California, Davis, Kansas State University.
What skills is Earl Meierhenry known for?
Earl Meierhenry has skills like Pathology, Drug Development, Toxicology, Clinical Development, Cro Management, Good Laboratory Practice, Ind, Standard Operating Procedure, U.s. Food And Drug Administration, Clinical Study Design.
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