11 November 2009, Helsinki-Vantaa, Finland
New requirements for medical devices and software – what changes on 21.3.2009? (in Finnish)
Presentations on:
Direktiivin 2007/47/EY (medical devices) sisältö ja merkitys alan eri toimijoille (The contents and significance of Directive 2007/47/EC to different stakeholders in the field)
Laiteluokittelu, raja-alueet, tulkintaohjeet, MEDDEV-oppaat – mitä uutta on tulossa (Device classification, borderlines, guidance, MEDDEV documents [...]
8 October 2009, Stockholm, Sweden
TOPRA Medical Devices Symposium
Presentation on “The Borderline and Classification Work Group – Industry Perspective”
7 – 9 September 2009, Cambridge, UK
Medical Device Summer School
Lecture and practical session on “Medical Device Classification”
11 March 2008, in Stuttgart, Germany
Medtec Europe
Chaired Session on “Changing Requirements in Europe (Directive 2007/47/EC and New MEDDEV on Vigilance)”
Presentation on “Changes in Classification and Legal Regime Borderline”