Jose A.

Jose A. is a MedTech regulatory expert specializing in FDA, EU MDR, and global approvals, with a focus on SaMD and AI compliance. Currently serving as a Senior Regulatory Affairs Consultant at Abbott, they have secured over 130 global regulatory approvals for Class II and III medical devices by developing robust, audit-ready Quality Management Systems. Jose A. has previously held leadership roles at Peerbridge Health Inc., Baxter Healthcare Corp, and LaserSight Technologies, and has extensive experience in regulatory due diligence that significantly reduces compliance risks for investors and startups. They earned their degree from the Maryland University of Integrative Health between 2018 and 2020.