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Scope General This guideline incorporates ergonomics into a step-by-step process for the optimal design of office systems, including the design of jobs and work organization, layout of the office, environmental conditions...

This document specifies requirements for test organisms, suspensions, inoculated carriers, biological indicators and test methods intended for use in assessing the performance of sterilizers and sterilization processes...

These requirements cover temporary lighting strings rated not more than 20 A, 125 V, intended for indoor and outdoor use to provide temporary illumination during the period of construction, remodeling, maintenance, repair, or...

1.1 These requirements apply to Factory-Built Type A Chimneys, which do not require field fabrication. They are for use with gas and liquid fuel-fired residential appliances and building heating equipment, where the appliance...

Note: The title and scope for this NOI was updated by the responsible SDO on March2 ,2021 (originally published July 14, 2020) 1.1 These requirements cover mechanical type accessories that are typically intended for...

1 Scope 1.1 These requirements cover mechanical type accessories that are typically intended for attachment to storage tanks or connecting pipe for flammable and combustible liquids in commercial (public) or private (fleet)...

This part of ISO 9241 provides guidelines to users of VDT-based information processing systems with reference to office tasks. This guidance is relevant to both the organization implementing the system and the people using...

1. Scope This part of ISO 9241 provides guidelines to users of VDT-based information processing systems with reference to office tasks. This guidance is relevant to both the organization implementing the system and the people...

This document specifies requirements and good practice recommendations for the collection and transport of samples intended for medical laboratory examinations. This document is applicable to medical laboratories and service...

1.1 Inclusions 1.1.1 La présente Norme internationale spécifie les exigences relatives au développement, à la validation et au contrôle de routine d'un procédé de stérilisation à la chaleur sèche pour les dispositifs médicaux...