Setting up your ISO 13485 quality system
Wed, 18 Mar
|By webinar. Register for details
Every manufacturer of active medical devices must have a quality system in place. This webinar outlines the processes and best practices in getting your system ready for audit.
Time & Location
18 Mar 2020, 12:00 pm – 1:00 pm AEDT
By webinar. Register for details
About the event
The most important standard in MedTech is the ISO 13485 standard on quality management systems for medical devices. This standard sets out the requirements for regulatory purposes.
The founder of Ora Innovations, Kevin Badin, will outline what companies need to do to successfully establish their quality systems for medical devices.
Ora Innovations provides services for quality management, regulatory affairs, product development, product licencing and WHS. Kevin has over 20 years of experience in quality management systems in a range of industries.