Delivered by experienced quality and GMP (Good Manufacturing Practices) compliance consultants from SeerPharma, this valuable upskilling opportunity provides MedTech professionals with the knowledge needed to facilitate the implementation of an effective quality management system aligned with ISO 13485:2016.
ISO 13485:2016 specifies requirements for a quality management system where an organisation needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements.
Sponsored by the Victorian Medtech Skills and Devices Hub (VMH), this four day workshop is for Victorian-based Medical Device, MedTech and HealthTech organisations planning to provide medical devices and related services that consistently meet customer and applicable regulatory requirements of ISO 13485.
