Legal Ethics Expert Witnesses in North Carolina

This highly qualified attorney has been studying legal ethics for over 40 years. He earned his BA cum laude from Carleton University, his LLB summa cum laude from the Université de Sherbrooke, and his LLM from Yale Law School. Additionally, he was Columbia University's Law and Economics Fellow in 1981. Before coming to the US and entering academia, he served as a law clerk for a member of Canada's Supreme Court. He also served for five years on Quebec's Human Rights Commission. He sits on the advisory boards of several other think tanks. He sits on the Board of Governors of the National Association of Scholars. He or his op-eds have appeared in varied electronic media (including CNN, CNNfn, C-Span, Fox News, Fox News Online, Hudson Institute Online, National Public Radio, National Review Online, Tech Central Station, Voice of America, C.BC, Radio-Canada, and West German Radio) as well as in a wide array of newspapers (including the Wall St. Journal, Christian Science Monitor, Baltimore Sun, Washington Times, Tulsa Journal, Kansas City Star, [Montreal] La Presse, Montreal Gazette, [Montreal] Le Devoir, [Toronto] Globe and Mail, and Japan Times). Currently, he is a Professor of Law at a VA university where he teaches Torts, Legal Ethics, Products Liability, and Jurisprudence. His research on torts and ethics issues is nationally known has published numerous books, chapters, and articles on legal ethics. Notably, he is co-author of two editions of West's Legal Ethics in a Nutshell and is sole author of two editions of West's Products Liability hornbook.

This expert's professional career has spanned 50 years, while for the past 20 years he has specialized in guiding companies through the CE marking process for products prepared to enter the EU market and for companies in the US who want CE marking on their products for market flexibility and/or liability protection, many of which are medical devices and machinery. This expert conducts forensic legal analysis of companies' Quality Management Systems (ISO 9001), Environmental Management Systems (ISO 14001), and Quality System Regulations as stipulated by the FDA. He has hosted over 450 seminars and workshops and has published more than 300 articles and multiple books in the areas of Liability, EU Directives/CE Marking, Technical Standards, FDA Quality System Regulations, and ISO 90001 and 14001. He has developed and delivered on-site training programs on product liability exposure for medical device insurance companies, as well as for corporate counsel, defense counsel, and trial attorneys involved with medical devices and medical device manufacturers. As a Senior Consultant for both Excel Partnerships and SAI Global, he also developed and delivered on-site training programs on CE marking for the Medical Devices Directive and related Quality Management Systems. As Legal Expert/Expert Witness he has prepared legal materials for use in litigation involving Quality Systems and CE marked products as well as EU Administrative Reviews.