Medtech Insight is part of the Business Intelligence Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

New Guidelines For Device Modelling And Simulation Up For Trilogue Discussion

This article was originally published in Clinica

Executive Summary

Changes made by the Council of the European Union to the European Commission’s proposed Medical Device Regulation include a requirement for notified bodies to take into account modelling and simulation activities carried out by the company applying for CE marking approval.

Advertisement

Topics

Advertisement
UsernamePublicRestriction

Register