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ICS:11.040.01
Showing 28–31 of 31 results
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ISO 15223:2025 Medical devices – Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements – Amendment 1: Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specific
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ISO 15223:2021 Medical devices – Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements
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ISO 15378:2024 Primary packaging materials for medicinal products – Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) – Amendment 1: Climate action changes
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ISO 62366:2016 Medical devices – Part 1: Application of usability engineering to medical devices – Technical Corrigendum 1
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