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    • Training

      Qity offers a wide range of on-site or remote training sessions to help your team master critical skills and stay ahead in a fast-changing industry. Our experts will teach your team how to design, develop and manufacture your device in compliance with regulatory standards.

    • Essential Training for Life Science Professionals

      Our courses build the foundational and advanced skills required to navigate the complexities of modern product development.

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      Taught by Industry Experts

      Our trainers aren't just instructors; they are seasoned professionals with deep experience in medical device and laboratory equipment industries. They provide practical insights and real-world knowledge you can't get from a textbook.

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      Practical, Hands-on Sessions

      We believe in learning by doing. Our training sessions are interactive and include hands-on exercises, allowing your team to apply new concepts to their own projects immediately.

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      Certified Training

      Our courses are designed to not only build skills but also to help you demonstrate to auditors and regulators that your personnel are officially qualified and up-to-date with the latest standards.

    • Training Portfolio

      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.

      Good Clinical Practice

      Learn how to conduct clinical studies in compliance with good clinical practice guidelines per ISO 14155 for devices and ICH GCP E6 for drugs.

      Jira

      Learn how to organize your work, automate processes and manage projects in Jira.

      Confluence

      Learn how to organize, find and collaborate on documentation in Confluence.

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