Clinical Research Update Seminar
With this seminar series, we want to keep you up to date on new developments and current topics in clinical research. We explain changes in current laws, discuss new national or international regulations and processes, and introduce new working methods and tools.
Seminar language is usually German.
Clinical research with medical devices - what is changing?
With the entry into force of the revised Swiss medical device law on 26 May 26 2021, some changes for clinical research with medical devices will arise.
In our update seminar on 10 March 10 2021, experts gave an overview. Here you will find recordings of the individual presentations. Presetations were given in German.
![[Translate to English:] KlinV Mep](/fileadmin/_processed_/8/e/csm_AdobeStock_291011817_05fcfa9a45.jpeg?1617008774)
Hintergründe zur europäischen Medical Device Regulation (MDR)
Prof. Roger Abächerli, PhD, Institut für Medizintechnik, Hochschule Luzerz, Referent und Trainer TüV Süd Akademie
Die MDR und ihre Implikationen für die klinische Forschung in der Schweiz
Claudia Becherer, DAS, Teamleiterin Regulatorik, Departement Klinische Forschung (DKF), Universität Basel
Die Umsetzung der MDR im klinischen Forschungsalltag
Daniela Penn, Clinical Research Manager, Regulatory Affairs Manager, Quality Manager, medXteam GmbH Neustadt an der Weinstrasse
Entwicklung von Medical Device Software in der Praxis
Prof. Phillippe C. Cattin, Leiter Departement Biomedical Engeneering (DBE), Universität Basel
Services des DKF für Forschungsprojekte mit Medical Devices
Roland John, Teamleiter Quality Affairs, Departement Klinische Forschung (DKF), Universität Basel
For questions regarding this or upcoming Clinical Research Update Seminars please contact Sandra Kohlmaier, PhD, Senior Scientific Officer Training and Education at the DKF.