IEC 60601-1 as part of Medical Device Design and Testing
During the training we will open the content of the IEC 60601-1 series of standards in terms of technical requirements. We review IEC 60601-1 as part of its approvals for different markets. From IEC 60601-1 ed. 3.2, we provide you with an understanding of testing, electrical safety and risk management requirements for medical devices. All of which are key considerations in the design and testing of medical devices.
Our training course will provide you with a comprehensive understanding of risk management, which strongly guides the requirements, design, testing and documentation of medical devices. We also handle the requirements for the accompanying documents and design documentation from a testing point of view. We also open up the future and need for change of IEC 60601-1.
Training is conducted in Finnish.