Events

Webinar | The Notified Body Role & The Conformity Assessment Process  

CORE–MD final event

The CORE-MD consortium is organising its Final Conference on Friday 15 March 2024 at the De Warande Club in Brussels. This event will gather representatives from regulators, notified bodies, researchers, industry but also patients and healthcare professionals. It will notably contribute to share its insights on the clinical evaluation of high-risk medical devices based on the work done by […]

Webinar | Recommendation for clinical evidence generation 

Webinar | CORE MD Recommendation on registries

Webinar | Early clinical investigations of new high-risk medical devices – a review of European experience.

The CORE-MD Consortium organised it’s tenth webinar for Monday 8 of January 2024. The title of this webinar is “Early clinical investigations of new high-risk medical devices – a review of European experience.”

Webinar | Providing high-risk medical devices for children – problems and proposals

The CORE-MD Consortium has organised it’s ninth webinar and last webinar of 2023 for Thursday 14 of December. The title of this webinar is “Providing high-risk medical devices for children – problems and proposals” REPLAY:

Webinar | IT tools for regulatory science: aggregating available data for assisting Expert Panels and improving post-market surveillance

The CORE-MD Consortium has organised it’s eighth webinar for Tuesday 05 of December. The title of this webinar is “IT tools for regulatory science: aggregating available data for assisting Expert Panels and improving post-market surveillance“ Moderator: Prof. Alan Fraser The Webinar will address the following topics: Learning Objectives:

Webinar – Pivotal Clinical Investigations of High-Risk Medical Devices: “What Guidance Do We Need and by Whom?”

The CORE-MD Consortium has organised it’s seventh webinar for Monday 27 of November. The title of this webinar is “Pivotal Clinical Investigations of High-Risk Medical Devices: “What Guidance Do We Need and by Whom?”. Moderator: Prof. Alan Fraser The Webinar will address the following topics: Learning Objectives:

Workshop on “Methodologies for evaluating high-risk medical devices: a matrix of study designs”

Workshop on “Methodologies for evaluating high-risk medical devices: a matrix of study designs” The CORE-MD consortium have produced extensive reviews of clinical evidence and scientific validity of different study designs and evaluation methodologies along the medical device life-cycle – from pilot observational studies to large randomised controlled trials and including new methodologies. These results are […]

Workshop on “An Ethics Charter for medical device innovation”

Workshop on “An Ethics Charter for medical device innovation” Innovators and academic medical scientists who are involved in the development, testing, and initial clinical evaluation of new high-risk medical devices face particular challenges.In that context, a charter that defines the essential principles of ethical practice would clarify how issues such as unknown risks, requirements for […]