DVM (Paris, France).

PhD, Comparative Pharmacology & Toxicology, University of California.

Additional Education: Dermatology, Ophthalmology, Carcinogenicity, Advanced Clinical Research Associate,  Food Sanitation and Inspection, etc.

• Drugs: Convetional, Nanoparticles,
• Medical Devices
• Biocompatibility ISO 19883, FDA G95-1
• Oncologics 
• R&D/Regulation and Support.
• Carcinogenicity.
• Environmental Safety Assessment. 
• Dermatologicals,
• Ophthalmologicals. 
• Litigation,
• Arbitration.
• GLP. 
• Licensing.
• Study outsourcing and monitoring. 
•  Preparation of IND, NDA, IDE, PMA 
• Toxicology profiles, MSDS, Monographs. 
• Consumer product and Industrial chemicals. 
• Literature search and analysis.
• USA and EEC citizen.
• Multilingual. 

• Former Director/Div of Toxicology/FDA, and leading, multinational drug companies (Merck, Bristol-Myers), CROs.
•  Long experience in Toxicology and Pharmacology/Regulation. 
• Senior Consultant (Since 1991) for numerous Pharmaceutical/Cosmetic companies and several Law firms.
•  Regulatory strategies.
• Review and preparation of regulatory documents, and expert reports.
•  Pharmaceutical industry representation at  FDA.
• Author of numerous  publications, reports and presentations on drug safety and efficacy, and extensive proprietary work.
• Member of 20 professional associations.
• Recipient of multiple wards, distinctions, and biographical citations.
• Food Safety.
• GLP compliance (since 1978), and Inspection.