Training
Qity offers a wide range of on-site or remote training sessions, targeted at medical and laboratory device manufacturers.
Our experts will teach your team how to design, develop and manufacture your device in compliance with regulatory standards.
Training Portfolio
Confluence
Learn how to organize, find and collaborate on documentation in Confluence.
Jira
Learn how to organize your work, automate processes and manage projects in Jira.
Quality Management Systems
(ISO 13485)
Train your team on the fundamentals of a Quality Management System for medical and in-vitro devices.
Software Development
(IEC 62304)
Learn how to establish a software development lifecycle for medical and in-vitro devices.
Basic Safety & Essential Performance
(IEC 60601/61010)
Learn how to demonstrate basic safety and essential performance for medical and laboratory equipment.
Usability Engineering
(IEC 62366)
Learn how to establish a human-centric usability engineering process for the design and evaluation of medical and in-vitro device user interfaces.
Risk Management
(ISO 14971)
Learn how to manage risks throughout the lifecycle of a medical or in-vitro device.
Cybersecurity & Data Privacy
Learn how to manage Cybersecurity risks for medical devices, and how to manage confidentiality, integrity and availability of your data.
Software Validation
(ISO 80002)
Learn how to validate software in compliance with EU and FDA regulations and guidelines.