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Medical Devices – An Introduction to Product and Company Development in a Regulated Environment
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 involved in product development and sales, business owners, founders, and CEOs, this course offers an in-depth overview of implementing a quality management system (QMS) and…
Medical Software Regulatory Requirements – 1-Day Workshop
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 equip you with foundational knowledge in regulatory standards for medical software, addressing both "software as a medical device" (SaMD) and software integrated within medical devices…
1-Day Intro to ISO 13485 Quality Management Systems (QMS)
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 standard, this course will guide you through understanding how to define the scope of a QMS, the core principles behind ISO 13485, and how processes…