What are Common Specifications within MDR & IVDR? [Stefan Bolleininger]
What are Common Specifications Under EU MDR and IVDR?
EU MDR Annex XVI - Draft Common Specification [Stefan Bolleininger]
-Implementing Act IVDR Common specification - Consultation until Sept 16th
Fast Facts - What is the MDR?
TÜV SÜD MDR interpretation: Devices with both medical and non-medical intended purpose (Annex XVI).
What can we learn from the first MDR audits with Martin Witte (TÜV SÜD)
Introduction to the European MDR 2017 745
MDR Technical Documentation Requirements | MDR and IVDR Compliance Webinar
Top 7 CE Class IIa Certification Mistakes & How to Avoid Costly MDR Pitfalls
Understanding the MDR & IVDR: What Medical Device Companies Need to Know.
１章 欧州医療機器規則MDR（Medical Device Regulation）
Why do we need IVDR Class D Common Specification with Andreas Stange
２章 欧州医療機器規則MDR（Medical Device Regulation）
Free webinar on Medical Devices Regulation - MDR & MDSAP
Medical Device News - December 2022 update
MDR Effects on Medical Device Processing
MDR Series: TIPS with ISA. Tip 1: Finding and Use of Harmonized Standards in EU MDR Regulation.
１章 MDR・IVDRの最新情報及び臨床評価
Frequently Asked Questions on Annex XVI products (MDR 2017/745)
