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Visit the CMDT website for links to upcoming webinars, workshops, and other events happening across the NZ ecosystem.
Visit the CMDT website for links to upcoming webinars, workshops, and other events happening across the NZ ecosystem.
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This regulatory workshop is provided in collaboration with Te Tītoki Mataora. Aimed at pre-spinout research groups and early-stage startups, this workshop covers the fundamentals of quality and regulatory considerations for medical devices.
This regulatory workshop is provided in collaboration with Te Tītoki Mataora. Aimed at pre-spinout research groups and early-stage startups, this workshop covers the fundamentals of quality and regulatory considerations for medical devices.
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Join this interactive workshop covering the regulatory aspects of SaMD and SiMD products. The workshop is aimed at researchers and early-stage companies who are developing medical devices that contain software (SiMD) or software as a medical device (SaMD).
Join this interactive workshop covering the regulatory aspects of SaMD and SiMD products. The workshop is aimed at researchers and early-stage companies who are developing medical devices that contain software (SiMD) or software as a medical device (SaMD).
This market validation workshop is aimed at early stage healthtech companies, or healthtech companies that would like to have a fresh look at their market and how they have validated it to date.
This market validation workshop is aimed at early stage healthtech companies, or healthtech companies that would like to have a fresh look at their market and how they have validated it to date.
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Are you ready to learn how to turn ISO 13485 from a regulatory obligation into a strategic advantage? Join us for the third webinar in the Quality Management Series: Driving Quality Forward – Risk & Efficiency Strategies for ISO 13485 Success. In this session Anne Arndt, will share practical insights on: How risk management can drive a proactive QMS; how lean implementation cuts complexity and cost; and how strong compliance can accelerate market access and strengthen your competitive position
Are you ready to learn how to turn ISO 13485 from a regulatory obligation into a strategic advantage? Join us for the third webinar in the Quality Management Series: Driving Quality Forward – Risk & Efficiency Strategies for ISO 13485 Success. In this session Anne Arndt, will share practical insights on: How risk management can drive a proactive QMS; how lean implementation cuts complexity and cost; and how strong compliance can accelerate market access and strengthen your competitive position
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