MDR and IVDR – The evolving challenges of EU regulations

Understanding the MDR & IVDR: What Medical Device Companies Need to Know.Подробнее

MDR and IVDR update: Overview and status of EU and national implementationПодробнее

An Overview of the EU Medical Device Regulation MDR and In Vitro Diagnostics Regulation IVDR PREVIEWПодробнее

Navigating the EU Medical Device Regulation 2017/745Подробнее

EU Medical Device Regulation WebinarПодробнее

MDR & IVDRПодробнее

Did extension of the EU Medical Device Regulations (MDR) really give you more time?Подробнее

EU MDR Challenges and RisksПодробнее

Implementing the EU MDR and IVDR with Oxford Global ResourcesПодробнее

The Impact of EU MDRПодробнее

Analysis of EU MDR & IVDR Amendment Proposal 2023/0005 - CelegenceПодробнее

CAPTIS™ - Technology for EU MDR & IVDR ComplianceПодробнее

FAQ Medical Device Economic Operators ? (EU MDR and IVDR)Подробнее

Regulatory Strategy MD & IVDПодробнее

Readiness for EU MDRПодробнее

Mastering the EU MDR & IVDRПодробнее

CAPTIS™ - Technology for EU MDR & IVDR ComplianceПодробнее

The New EU MDR PMS Requirements WebinarПодробнее

Current Challenges in MDR (Medical Device Regulation) in the EU - Webinar with NO-FEAR ProjectПодробнее