This event is the only pan-European and English-language conference that is dedicated to the important area of software design in the Medical Device industry. The event will address the key issues in development, regulation and compliance; including:
Building more effective usability/human factors methodologies into software development
Making your development processes more agile, and improving your agile standards compliance
Getting the latest regulatory updates from the perspective of the Notified Bodies – how does their interpretation of the standards such as IEC 62304 differ from yours? What do they expect?
Ensuring the interoperability and security of your devices in order to enhance and protect them in the user environment
Managing the requirements and differences in the upcoming IEC 6601 3rd edition – are you compliant?
Book your place today!