Guidance on the relationship between EN ISO 13485: 2016 (Medical devices - Quality management systems - Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation
Document status: [ Active ]
High-voltage switchgear and controlgear Part 307: Guidance for the extension of validity of type tests of AC metal and solid-insulation enclosed switchgear and controlgear for rated voltages above 1 kV and up to and including 52 kV
Document status: [ Revised ]
Apparecchiature ad alta tensione Parte 307: Guida per l’estensione della validità delle prove di tipo per apparecchiatura prefabbricata a corrente alternata con involucro metallico o in materiale isolante solido per tensioni nominali da 1 kV a 52 kV compreso
Document status: [ Active ]
Field device tool (FDT) interface specification Part 51-150: Communication implementation for common object model - IEC 61784 CPF 15
Document status: [ Active ]
Field device tool (FDT) interface specification Part 52-150: Communication implementation for common language infrastructure - IEC 61784 CPF 15
Document status: [ Active ]
Field device tool (FDT) interface specification Part 52-31: Communication implementation for common language infrastructure - IEC 61784 CP 3/1 and CP 3/2
Document status: [ Active ]
Field device tool (FDT) interface specification Part 52-32: Communication implementation for common language infrastructure - IEC 61784 CP 3/4, CP 3/5 and CP 3/6
Document status: [ Active ]
Field device tool (FDT) interface specification Part 52-90: Communication implementation for common language infrastructure - IEC 61784 CPF 9
Document status: [ Active ]
Radiation protection instrumentation - Determination of uncertainty in measurement
Document status: [ Active ]
OPC unified architecture Part 1: Overview and concepts
Document status: [ Active ]
