Finland updates device regulations in line with new law
This article was originally published in RAJ Devices
Executive Summary
Finland's National Supervisory Authority for Welfare and Health, Valvira, has issued four administrative orders regulating the procedures for medical device incident reporting, registration and clinical trials, in line with new medical devices legislation that came into force earlier this year1. The updated rules, which are expected to help manufacturers and other stakeholders better understand the various requirements, came into effect on 15 September.