Here's your chance to fast-track your product's market entry with Johner Institute New Zealand's cutting-edge Regulatory Strategy Course. Designed for medtech professionals and newcomers looking to make their mark in…
Embark on a 6-month journey with Johner Institute New Zealand to master the intricacies of ISO 13485 and FDA 21 CFR 820 compliance through our Quality Management System (QMS) course,…
Discover how to successfully bring a medical device to market in this comprehensive 2-day introductory course by the Johner Institute New Zealand on 20 and 28 November. Designed for those…
The Johner Institute New Zealand, in collaboration with Te Tītoki Mataora and HealthTech Activator, is pleased to present the "Medical Software Regulatory Requirements" workshop in Auckland. This hands-on workshop will…
This 1-day course provides a comprehensive introduction to ISO 13485, the international standard for quality management systems in the medical device industry. Instead of focusing on individual sections of the…
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