About this document
Guidance on ISO/TR 24971 Application by brusson is a document available to read on EtoBox.
ISO/TR 24971:2020 provides guidance for manufacturers on developing, implementing, and maintaining a risk management process for medical devices in accordance with ISO 14971:2019. The document outlines the risk management process, including risk analysis, evaluation, control, and post-production activities, and is structured to align with ISO 14971:2019 for ease of use. It includes informative annexes that offer additional guidance on specific aspects of risk management relevant to various types of medical
- Author
- brusson
- Language
- EN