Extensions for EU MDR and IVDR Implementation
Extensions for the European Union MDR and IVDR Key EU medical device regulation updates Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation My Account Contact Initial EU MDR and IVDR transition periods extended In 2023,...Implementation of the EU MDR and IVDR
Implementation of the European Union MDR and IVDR Key EU medical device regulation updates Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation My Account Contact A Significant EU Regulatory System Overhaul The...Regulatory Documentation for National and Global Market AccessÂ
With a solid base of technical documentation, our regulatory specialists will prepare a regulatory submission that is organized, well written, complete, and meets the regulatory requirements of the agency that will evaluate the product.