Alexandre Petiard

He specializes in high-risk submissions, clinical evaluations, risk management, and global strategy for implantable devices across cardiology, orthopedics, and neurosurgery. Petiard is an experienced trainer and auditor with expertise in global regulations and standards, including the MDD and MDR, ISO 13485, FDA QSR, Brazil GMP, MDSAP, and risk management to ISO 14971:2019.Prior to joining Pure Global, Petiard held positions at Cactus Life Sciences, Emergo by UL Solutions, and Covidien (now Medtronic). He holds a degree in biomedical engineering from ISIFC in France.