Analysis of EU MDR & IVDR Amendment Proposal 2023/0005 - Celegence
EU MDR and IVDR consolidated versions
The New EU MDR PMS Requirements Webinar
MedTech Chats: A Look Inside the New EU Medical Device Regulation (MDR)
How to build a winning strategy for EU MDR Compliance & Medical Device Regulatory requirements
Medical Device News - August 2020 review (without Clip)
Medical Device News - July 2020 Update - EU MDR and IVDR
新しい MDR による医療機器クラス I - 正誤表 2 (パート 1/2)
Medical Devices Regulations (MDR) 2020 - presentation by Tony Griffin
Medical Packaging Regulatory & Standards Update (March 31, 2020)
FAQ 医療機器経済事業者? (EU MDR および IVDR)
Notified Body overview
Medical Device News - June Update 2021 [EU MDR date of Application]
Is the EU MDR now extended? What if your certificates already expired?
1 year delay for EU MDR 2017/745 with Erik Vollebregt (Medical Device)
Medical device regulation and the MHRA devices registration system
How to Prioritize Documentation for MDR Transition Planning
What should verify the Economic Operators? (EU MDR and IVDR)
Medical Device News - August 2021 Regulatory Update [MDR & IVDR]
Workshop: How to write your Intended Purpose? [Medical Device case study]