Electrical and EMC Safety in IVD Medical Devices

Electrical and EMC Safety in IVD Medical Devices  

What should be considered in the requirements for an In Vitro medical device from the perspective of electrical safety and EMC? What requirements must be met before placing the product on the market? In this training, we will review the most essential requirements from the electrical safety and EMC standards EN 61010 and EN IEC 61326.

The training is intended for individuals responsible for product development and procurement (e.g., components), quality, documentation, sales, and after-sales in companies manufacturing medical devices. The training will be conducted in Finnish, but the training material will be in English to familiarize participants with the terminology and allow room for interpretation of the standards.
This training provides essential information on the standard requirements for electrically powered In Vitro medical devices. Welcome to hear what requirements your IVD device should meet.

Training is conducted in Finnish.