Global Medical Devices RA and PV capabilities

At the Medical Devices Global Regulatory Affairs and Pharmacovigilance division, the team offers end-to-end solutions to ensure that medical devices comply with regulatory requirements around the world. The team of experienced regulatory and pharmacovigilance professionals understands the complex and ever-changing landscape of medical device regulations, and they are committed to guiding clients through the process from concept to post-market surveillance. The team offers a full range of regulatory and pharmacovigilance services, including product classification, regulatory strategy development,