Brian T. McVerry, Ph.D.

Brian T. McVerry, Ph.D. is a medical device development and regulatory strategy expert specializing in technology development, licensing, and FDA regulatory compliance. With a career encompassing chemistry, biomaterials, and implantable device design, he brings a multidisciplinary approach to evaluating complex medical device cases. His work centers on investigating regulatory compliance, assessing technology development processes, and evaluating whether industry standards have been met in medical device disputes.

Mr. McVerry has been retained in numerous expert witness and consulting engagements across the United States, involving medical device development, regulatory compliance, and patent disputes. His Ph.D. in Chemistry, along with his extensive experience in technology development and FDA regulatory strategy, reinforce his ability to deliver objective, defensible analyses. He is regularly engaged by both plaintiff and defense counsel to provide clear, independent determinations of regulatory compliance and standard of care in disputes involving medical device technologies.