English (United States)

SAVE THE DATE A Multi-Stakeholder Workshop of the Joint EFGCP-MedTech Europe Medical Technology Working Party

reduce font Size enlarge font Size print content

Organised by: EFGCP & MedTech Europe

The upcoming European Regulation on Medical Devices will change the landscape for the development of medical devices. This multi-stakeholder workshop will offer the floor for an exchange of views and opinions on topics of particular complexity and input to the relevant decision-makers.
Setting effective ethical and quality clinical standards for medical technology studies is critical to ensuring that patients have access to safe and effective treatment. For the first time, patient representatives, healthcare providers, ethicists, competent authorities, industry and policymakers will be able to present and discuss their needs and expectations, the options and opportunities for mitigating risks in the development and full life cycle of medical devices and the best ways of building clinical evidence.


* Understand the differences between clinical trials with medicines and medical devices
* Identify suitability of concepts and lessons learned in medicines development for clinical development of
   medical devices
* Discuss how best to ensure the required ethical and quality standards in medical device trials


Programme and more information are available here: www.luxclin.lu/Events/Details/?c=EVT8030EQK

Who should register?

Healthcare professionals who wish to be part of a unique network, providing access to up-to-date, accurate and validated information about clinical research.

Investigators and study staff who wish to be part of a unique network, in order to stay abreast of clinical trials taking place in Luxembourg and who are willing to further develop their competencies.