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The HealthTech Activator and Te Tītoki Mataora are pleased to host our first workshop on the regulation requirements for Software as a Medical Device (SaMD) products. This one-day, compact workshop aims to increase your competence in the practical implementation of regulatory requirements (in particular, IEC 62304) while promoting efficient software development. It is an introduction to the topic of development, quality assurance and approval of medical software (software as a medical device or medical device software).
This workshop will help you:
Event details:
Date/time: Thursday 2 March, 9:00am-4:00pm
Location: Auckland Bioengineering Institute, The University Of Auckland, 70 Symonds Street #6, Auckland