Brochure
Medical Devices

Ethical and Trustworthy Artificial Intelligence

BSI’s introduction to the European Artificial Intelligence Draft Act (AIA).

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In this document:

Defining AI and its purpose.
Prohibited AI practices.
Requirements and obligations.
Conformity Assessment.

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EU MDR – Post Market Clinical Follow-Up

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Using Standards to Demonstrate Conformity

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Annex XVI - Devices Without an Intended Medical Purpose

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Unlocking the Potential of Consumer Wearables in Healthcare

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Medical Device Lifetime - Assisting manufacturers

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AI Machine Learning and Medical Devices

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