ISO 50001 Certification News - DNV

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X [Thermal Power plant KOSTOLAC, SERBIA] Sucessfully certified to ISO 50001 Sustainability, Green Initiatives and Ecology 1
R ISO 50001 Awareness Training Requirements Training - Internal, External, Online and Distance Learning 9
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R Energy Baseline in ISO 50001:2011 Sustainability, Green Initiatives and Ecology 1
A Auditor Man-Day table for ISO 50001 (Energy Management Systems) Sustainability, Green Initiatives and Ecology 3
S What is the future of ISO 50001 EnMS (Energy Management Systems)? Miscellaneous Environmental Standards and EMS Related Discussions 3
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M ISO 50001 Energy Management Lead Auditor Training Training - Internal, External, Online and Distance Learning 4
M Free Webinars on ISO 50001 Energy Management - 2011 and 2012 Miscellaneous Environmental Standards and EMS Related Discussions 6
I EN 16001 or ISO 50001 - Which way would you go? Sustainability, Green Initiatives and Ecology 5
Randy ISO 50001 Energy Management Systems - Requirements Sustainability, Green Initiatives and Ecology 29
Sidney Vianna ISO 50001 released June 15 2011 Other ISO and International Standards and European Regulations 22
B Do IFU designs have to be document controlled under ISO 13485? Document Control Systems, Procedures, Forms and Templates 1
H ISO 13485 - Separate Microbiology Audits ISO 13485:2016 - Medical Device Quality Management Systems 1
M Case study help as per ISO 9001: 2015 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
M Case study solution help required as per ISO 9001 : 2015 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 0
C Production and Post Production feedback - ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 4
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D Test summary report example for design validation wanted - ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 1
J Informational ISO 24971:2020 Released ISO 14971 - Medical Device Risk Management 0
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M Risk Analysis Flow - Confusion between ISO 14971 and IEC 62304 IEC 62304 - Medical Device Software Life Cycle Processes 7
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N EN ISO 13640:2002 vs EN ISO 23640:2011 Other Medical Device Related Standards 1
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K ISO 15223-1 Do Not Reuse and Do Not Resterilize Other Medical Device Related Standards 5
A ISO 10002:2018 Checklist Needed (Complaints Handling) Customer Complaints 5
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