Regulatory guidance
Software as a Medical Device: Possible Framework for Risk Categorization and Corresponding Considerations
Published Sep 18, 2014
Reference
IMDRF/SaMD WG/N12
Source
IMDRF
Status
Final
Published
Sep 18, 2014
Languages
EN
This document has been translated to Spanish by an external agency. The translation may be accessed from the agency's site by the link below.Please note that translations are for reference purposes only and responsibility for the accuracy of the translation belongs to the translating agency.Translation by IACRO into Spanish may be found here.
Source: IMDRF. Read the full document on the official source.
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© International Medical Device Regulators Forum (IMDRF). Reproduced for non-commercial reference; see imdrf.org for terms.
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