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Software Validation in Medical Devices

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Software Validation in Medical Devices

Training Software validation for medical devices, in accordance with the updates in ISO 13485:2016 and ISO 14971:2019, is an essential part of the routine processes in the product lifecycle of medical device manufacturers. However, completing this task requires technical expertise. Solution partners become a necessity in this context. Through this training, manufacturers will gain awareness and be able to manage a more efficient process with their solution partners.

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