The SCTO’s Regulatory Affairs Platform organises a roundtable for the Swiss research community and authorities each year. This roundtable provides an important exchange platform to discuss with Swissmedic and swissethics issues and challenges related to the implementation of the Human Research Act (HRA).
Topics mainly cover the changing regulatory landscape at the European level, such as the EU’s General Data Protection Regulation (GDPR), Clinical Trial Regulation, or new medical devices regulations. Many different kinds of national challenges are addressed at the roundtable as well.hallo