MedTech: EU MDR Exchange
The EU MDR: Need Answers?
Software as a Medical Device Digital Week
Explore The Latest updates to Software Regulations for Medical Devices from the European Commission and Notified Bodies
EU MDR, IVDR & Global Market Regulations: Bringing The Latest Guidance To You
Biocompatibility for Medical Devices US
Navigate the evolving biocompatibility landscape for medical devices
Regulatory Affairs in Latin America for Medical Devices
Develop your understanding of the regulatory landscape in Latin America to ensure fast device registration
LLM Medical Law and Ethics
Analyse, interpret and apply the laws regulating the provision of healthcare with particular regard to ethical perspectives
Medical Device School
Gain a practical overview of the processes involved in bringing a medical device to market led by an expert faculty
Articles & Video
The EU MDR Delay and Implementation - MedTech eBook Series
Discover the challenges of EU MDR implementation and impacts of the delay on the medical device industry in this MedTech eBook.
MedTech Report 2020: EU MDR and IVDR Compliance
Download the MedTech Report 2020 on EU MDR and IVDR Compliance, based on 265 survey responses from industry insiders.
Clinical expectations of the EU MDR with TÜV SÜD and MedSmart
Clinical expectations of the EU MD: Matthias Fink from TÜV SÜD, and Dona Occhipinti from MedSmart discuss in this exclusive video interview.
How the changing EUDAMED timeline impacts implementation of the EU MDR - with Eudamed.eu CEO Richard HoulihanDiversity and Inclusion
SURVEY: Diversity, Equity and Inclusion in the Life Sciences 2021
Changes to the ISO 10993-23 and its impact on the medical device industry with NAMSAMedTech
EU Notified Body Association Takes Steps to Allay EC's Virtual Audit FearsEU MDR & IVDR
MDR and IVDR: Onsite or offsite audits? That’s the question.
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