Sustainable cities and communities – Environmental, social, and governance (ESG) indicators for citi...
A city’s Environmental, Social and Governance (ESG) profile is fundamental in building a sustainable, inclusive, and resilient future. This Standard creates an ESG indicators framework, that is designed to support city leaders to address risk, improve decision-making and enhance their ESG profile once equipped with high calibre data that is generated with globally standardized key performance…
Information technology — Automatic identification and data capture techniques — EAN/UPC bar code sym...
Manufacturers of bar code equipment and users of bar code technology require publicly available standard symbology specifications to which they can refer when developing equipment and software.
ISO/IEC 15420:2009 specifies the requirements for the bar code symbology known as EAN/UPC. It specifies EAN/UPC symbology characteristics, data character encodation, dimensions, tolerances, decoding…
Artificial intelligence — Data quality for analytics and machine learning (ML) — Part 5: Data qualit...
This document provides a data quality governance framework for analytics and machine learning to enable governing bodies of organizations to direct and oversee the implementation and operation of data quality measures, management, and related processes with adequate controls throughout the data life cycle. This document can be applied to any analytics and machine learning. This document does not…
Biodiversity – Requirements and guidelines for strategically and operationally addressing biodiversi...
This standard defines requirements and guidelines to help organisations understanding and mainstreaming biodiversity’s protection, conservation, the sustainable use of its components and the fair and equitable sharing of the benefits arising out of the utilization of genetic resources, within their activities.
This standard is suitable for all kind of organisations (e.g. economic operators,…
Biological evaluation of medical devices — Part 1: Requirements and general principles for the evalu...
This document specifies:
— the general principles governing the biological evaluation of medical devices within a risk management process;
— the general categorization of medical devices based on the nature and duration of their contact with the body;
— the evaluation of existing relevant data from all sources;
— the identification of gaps in the available data…
