Jeffrey Lohre is an experienced quality assurance and regulatory affairs professional with expertise in medical devices. His key areas of focus include biocompatibility, toxicity, chemical toxicological risk assessments, chemistry, and sterilization. Mr. Lohre served as a Principal Biologist for Edwards Lifesciences’ Quality Laboratories Ranges, and now assists companies ranging from startups to Fortune 500s with product development and production support for Class I, II, and III medical devices. He has worked with products including implantable bioprosthetic heart valves, ophthalmic implants, ventricular assist devices, hemodynamic monitoring catheters, therapy delivering catheters, insulin delivery systems and pumps, and surgical instruments.
Regulatory Pathways Group Inc.
a California corporation
Inquiries and general information:
info@regulatorypathways.com
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