EU MDR Labeling, IFU, UDI, & Eudamed

Among the many changes resulting from EU MDR are new requirements for labeling, instructions for use, UDI, risk assessment for hazardous substances, and transparency of product data through the Eudamed database. Establishing the systems and protocols for remediation of current products and compliance of new ones will be a complex, costly, and time-consuming process. Registration will open soon.