Medical Devices Expert Witnesses in Alabama

This qualified engineer obtained his BS in Civil and Structural Engineering and his MS in Management of Technology from Kennesaw State University and Southern Polytechnic State University. He is a certified Professional Engineer and is certified in OSHA requirements and engineering and surveying. He is a member of the National Society of Professional Engineers and the National Academy of Forensic Engineers. He has 8 Publications and is currently a Structural Design and Forensic Engineer at an engineering firm in the southeast. Some of his fields of expertise include forensic/failure and safety analysis, civil/structural design of public and private structures, and construction site accident investigations. A partial list of past subjects addressed include wood/concrete deck collapses, commercial/residential roof damage evaluations, excavation failures/incidents product liability, traffic accident reconstruction, mold source evaluation, construction cost estimating, hydrology/sewer studies, airport consulting, roadway design, geotechnical/subsurface investigations, construction materials failure analysis, structural analysis and design of various material components, scaffolding failures, water damage source evaluation, structural damage inspections, OSHA compliance evaluations, and concrete/asphalt pavement evaluation and design. Has an intimate knowledge of OSHA worksite regulations, and the various national building codes and standards for Industrial, Commercial and Residential structures.

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.