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ISO 11615:2017 establishes definitions and concepts and describes data elements and their structural relationships, which are required for the unique identification and the detailed description of Medicinal Products. Taken together, the standards listed in the Introduction define, characterise and uniquely identify regulated Medicinal Products for human use during their entire life cycle, i.e.…

ISO/TS 20443:2017 defines concepts and describes data elements and their structural relationships, which are required for the unique identification and the detailed description of Medicinal Products. Taken together, all ISO IDMP standards (ISO 11615, ISO 11616, ISO 11238, ISO 11239 and ISO 11240) define, characterise, and uniquely identify regulated Medicinal Products for human use from approval…

ISO/TS 20451:2017 defines the concepts required to associate pharmaceutical products with an appropriate set of PhPID(s) in accordance with ISO 11616. Pharmaceutical identifiers and elements are to represent pharmaceutical products as represented in a Medicinal Product as indicated by a Medicines Regulatory Authority. The suite of ISO IDMP standards can be applied to off-label usage of Medicinal…

The information in ISO/TS 16829:2017 covers all kinds of ultrasonic testing on components or complete manufactured structures for either correctness of geometry, for material properties (quality or defects), and for fabrication methodology (e.g. weld testing). ISO/TS 16829:2017 enables the user, along with a customer specification, or a given test procedure or any standard or regulation to select…

1.1 This Standard applies to newly produced, outdoor cooking specialty gas appliances (see Clause 3), hereinafter referred to as appliances, constructed entirely of new, unused parts and materials. Appliances submitted for examination under this Standard areclassified as portable or stationary. These products are not intended for commercial use. 1.2 This Standard applies to recreational…

counter-measures, and technologies that may effectively apply to the modern electronically based IACSs regulating and monitoring numerous industries and critical infrastructures. It describes several categories of control system-centric cybersecurity technologies, the types of products available in those categories, the pros and cons of using those products in the automated IACS environments,…

L'ISO 11365:2017 est applicable aux fluides difficilement inflammables à base d'esters phosphates de triaryle utilisés comme fluides hydrauliques de régulation pour turbines ou autres systèmes de régulation des centrales électriques. Ces fluides appartiennent à la catégorie HFDR de l'ISO 6743‑4[1]. L'objet de l'ISO 11365:2017 est: - d'assister l'opérateur…

ISO 10987-3:2017 gives requirements and relevant information for evaluating used earth-moving machines. It provides the means to evaluate a used machine, relative to the information provided by the manufacturer in the operator's manual, in order to verify that the used machine is functional as intended by the manufacturer. ISO 10987-3:2017 is applicable to earth-moving machines as defined in…

ISO 7250-1:2017 provides a description of anthropometric measurements which can be used as a basis for comparison of population groups and for the creation of anthropometric databases (see ISO 15535). The basic list of measurements specified in this document is intended to serve as a guide for ergonomists who are required to define population groups and apply their knowledge to the geometric…

ISO/TR 18570:2017 provides guidance on a supplementary method to that defined in ISO 5349‑1 for measuring and reporting hand-transmitted vibration exposures. The method defined in this document provides an improved assessment methodology for evaluating vascular hand-arm vibration risks (vibration white finger). This document does not apply for other health effects (e.g. sensorineural and…