BS ISO 14068-1:2023

Climate change management. Transition to net zero Carbon neutrality (British Standard)

This document specifies principles, requirements and guidance for achieving and demonstrating carbon neutrality through the quantification, reduction and offsetting of the carbon footprint. This document defines terms used in relation to carbon neutrality and provides guidance on the actions necessary to achieve and demonstrate carbon neutrality. In accordance with common practice, it uses the word “carbon” to refer to all greenhouse gases (GHGs) in compound expressions such as “carbon neutrality”. It is applicable to a wide range of subjects such as organizations (including companies, local authorities and financial institutions) and products (goods or services, including buildings and events). It is not intended to be used for territories (such as regions, countries, states or cities), including signatories to the United Nations Framework Convention on Climate Change (UNFCCC) when reporting national outcomes for the purposes of that Convention. This document establishes a hierarchy for carbon neutrality where GHG emission reductions (direct and indirect) and GHG removal enhancements within the value chain take priority over offsetting. It includes requirements for carbon neutrality commitments and making carbon neutrality claims. This document is GHG programme neutral. If a GHG programme is applicable, the requirements of that GHG programme are additional to the requirements of this document.

BS 7671:2018/A1:2020

Requirements for Electrical Installations. IET Wiring Regulations (British Standard)

BS EN 17141:2020

Cleanrooms and associated controlled environments. Biocontamination control (British Standard)

BS EN ISO 20417:2021

Medical devices. Information to be supplied by the manufacturer (British Standard)

BS EN ISO 13485:2016+A11:2021

Medical devices. Quality management systems. Requirements for regulatory purposes (British Standard)

BS EN ISO 14971:2019

Medical devices. Application of risk management to medical devices (British Standard)

This document specifies terminology, principles and a process for risk management of medical devices, including software as a medical device and in vitro diagnostic medical devices. The process described in this document intends to assist manufacturers of medical devices to identify the hazards associated with the medical device, to estimate and evaluate the associated risks, to control these risks, and to monitor the effectiveness of the controls.  The requirements of this document are applicable to all phases of the life cycle of a medical device. The process described in this document applies to risks associated with a medical device, such as risks related to biocompatibility, data and systems security, electricity, moving parts, radiation, and usability.  The process described in this document can also be applied to products that are not necessarily medical devices in some jurisdictions and can also be used by others involved in the medical device life cycle.  This document does not apply to:  — decisions on the use of a medical device in the context of any particular clinical procedure; or  — business risk management.  This document requires manufacturers to establish objective criteria for risk acceptability but does not specify acceptable risk levels.  Risk management can be an integral part of a quality management system. However, this document does not require the manufacturer to have a quality management system in place.  NOTE Guidance on the application of this document can be found in ISO/TR 24971. 

BS EN 60204-1:2018+A1:2025

Safety of machinery. Electrical equipment of machines General requirements (British Standard)

Not available

BS EN IEC 63000:2018

Technical documentation for the assessment of electrical and electronic products with respect to the restriction of hazardous substances (British Standard)

BS ISO 45001 / ISO 9001 / ISO 14001 - Occupational Health and Safety Requirements Package

BS ISO 45001 / ISO 9001 / ISO 14001 - Occupational Health and Safety Requirements Package

BS ISO 45001 / ISO 9001 / ISO 14001 - Occupational Health and Safety Requirements Package provides the requirements to implement an environmental, quality and occupational health management system. This package enables BS ISO 45001 to be easily integrated into an existing environmental or quality management system while also providing the foundation to implement a new management system. BS ISO 45001 / ISO 9001 / ISO 14001 - Occupational Health and Safety Requirements Package includes:

 
• BS ISO 45001:2018
 
• ISO 9001:2015
 
• ISO 14001:2015
 
• Improving Worker Safety in Global Supply Chains - (Value Added Content)
 
• ISO 9001:2015 and Beyond - (Value Added Content)
 
• ISO 9001:2015 for Small Enterprises - What to do? - (Value Added Content)
 
• ISO 14001:2015 - Environmental Management Systems - A Practical Guide for SMEs - (Value Added Content)

BS EN ISO 20417:2021

Medical devices. Information to be supplied by the manufacturer (British Standard)