Medical Devices – An Introduction to Product and Company Development in a Regulated Environment
Dates: 23 July & 29 July 2025 | 17 Sept & 25 September 2025
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Workshop – Developing Medical Software according to IEC 62304 (3 August 2023)
Join us for an insightful workshop centered on the regulatory landscape of Software in Medical Device (SiMD) and Software as a Medical Device (SaMD) products. This event is jointly presented by Te Tītoki Mataora and HealthTech Activator, key players in the health tech industry. Details and Location The workshop is scheduled for the 3rd of…
Workshop – Medical Software Regulatory Requirements (3 August 2023)
Presented in collaboration by The Johner Institute New Zealand, Te Tītoki Mataora, and HealthTech Activator Join us for an intensive exploration of regulatory requirements for Software in Medical Device (SiMD) and Software as a Medical Device (SaMD) products. This comprehensive workshop is a collaboration between The Johner Institute New Zealand, HealthTech Activator, and Te Tītoki…
Free Webinar: Unpacking the FDA’s New Cyber Security Legal Requirements for Medical Devices
Do you need help understanding the new US Food and Drug Administration’s (FDA) legal requirements for cybersecurity in medical devices? We’ve got you covered. On August 17th at 11 a.m. (NZST), join us for a free, one-hour webinar on “FDA Cyber Security: From Guidance to Legal Requirements”. This virtual event, conducted over Zoom, is designed…