We’re excited to kick off this month by announcing a series of informative workshops designed to support your journey in the health tech sector.
Covering key topics like commercial strategy, planning, and regulatory requirements for medical devices and software, these sessions are tailored to meet the needs of everyone—from early-stage startups to established companies. Whether you're just starting out or looking to scale, there’s something for you! Be sure to sign up below to secure your spot.
A new Medical Products Bill is being introduced to replace the Medicines Act 1981, bringing in modern, flexible regulations to improve access to safe and effective medical products for all New Zealanders. The Bill is expected to pass in 2026 and come into effect by 2028, ensuring a smooth transition for existing products.
A separate bill for natural health products will also be developed after consulting with the sector. Later this month, the Ministry of Health is hosting a webinar to discuss the Medical Products Bill and its potential impact. For more details and updates, visit their website.
For further details and to explore more, visit the HTA web portal. If you have any questions or need assistance, feel free to reach out—we’re here to support you at every step!
Upcoming HTA workshops
Commercial Strategy & Planning 6 November, 9am – 4.30pm, Auckland Navigating healthtech supply chains is challenging. This workshop is ideal for early-stage as well as in-market HealthTech companies planning to grow or accelerate sales after launch. You will walk away armed with knowledge about how to optimise your value chain, craft compelling propositions, and master the sales process. Led by Dan Hansen, who draws on his extensive experience in senior and board roles and his first-hand commercial experience in over 35 countries with many of the world’s most recognised companies.
Clinical Investigation Process for Medical Devices Workshop 19 November 12pm - 5pm & 20 November 9am-1pm, Auckland After a successful workshop earlier this year, we are bringing back the Clinical Investigation Process for Medical Devices workshop. Led by Julie Jones of BioValeo, Julie brings a wealth of experience in clinical research covering various therapeutic areas, investigational products, devices, and all trial phases. Run over two-half days, this workshop is ideal for medical device companies. Join us to elevate your understanding of the clinical investigation process and planning, regulations and compliance, sponsor responsibilities, and more.
Demystifying Quality & Regulatory 14 November, 9am-3pm, Auckland Aimed at pre-spinout research groups and early-stage startups, this workshop covers the fundamentals of quality and regulatory considerations for medical devices. Offered in collaboration with Te Tītoki Mataora (MedTech Research Translator) and led by Yaara Yarmut, Chief Regulatory Officer at Alimetry and Natalia Lopez, Chief Operations Officer at Kitea Health.
Medical Software Regulatory Requirements 26 November, 9am – 3pm, Auckland Aimed at researchers and early-stage companies developing medical devices that contain software (SiMD) or software as a medical device (SaMD). This interactive workshop covers the regulatory aspects of SaMD and SiMD products. Offered in collaboration with Te Tītoki Mataora (MedTech Research Translator) and led by Anne Arndt, CEO of the Johner Institute New Zealand Ltd.
Exciting developments continue to emerge across New Zealand's health tech landscape.
Scentian Bio is using smell receptors for real-time disease detection, while Avasa is tackling the challenges of microvascular surgery. Tautoko Tech is also making global strides in diabetes treatment and equitable healthcare solutions. We’re proud to have collaborated with these innovators and are excited to see their ongoing impact. Read more below for the full stories.
