ISO/TC 84/WG 16 - Drug delivery system requirements for paediatrics and other demographics
Exigences relatives aux systèmes d'administration de médicaments pour les patients en pédiatrie et plus âgés
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ISO/TC 84/WG 16 is a Working Group within the International Organization for Standardization (ISO). It is named "Drug delivery system requirements for paediatrics and other demographics". This committee has published 1 standards.
ISO/TC 84/WG 16 develops ISO standards in the area of Information technology. Currently, there are 1 published standards from this working group.
The International Organization for Standardization (ISO) is an independent, non-governmental international organization that develops and publishes international standards. Founded in 1947 and headquartered in Geneva, Switzerland, ISO brings together experts from 170+ member countries to share knowledge and develop voluntary, consensus-based standards that support innovation and provide solutions to global challenges.
A Working Group in ISO is a specialized group responsible for developing standards or technical work within a defined scope. These bodies bring together international experts to create consensus-based standards that support global trade, safety, and interoperability.
This document provides requirements and guidelines on the development of drug delivery systems intended for self-administration of medicinal products by the specific demographic group of paediatric patients who are performing some or all use steps required for their intended use. Use steps include any handling action performed after the patient has received the product; these can include but are not limited to: - transport – carrying the product while travelling (e.g. by walking, train, airplane, automobile, bus); - storage – storage by the patient in their home, school, office or in temporary storage cases before or between uses; - preparation – steps necessary to place the product in a state where it is ready to be administered; - operation – steps necessary to initiate, adjust, pause, stop, or otherwise manage the delivery of medication using the product; - maintenance – steps necessary to keep the product in good working order; - disposal – steps to ensure safe disposal of the product after use (e.g. placement of the product in a suitable receptacle). This document is applicable to injectable drug delivery systems for administration of medicinal products. Furthermore, this document can be useful for the development of other drug delivery devices or systems if they are intended for use by the paediatric population. Devices not in the scope of this document include catheters, for example those in the scope of ISO 10555 series, and infusion pump systems, e.g. IEC 60601-2-24 and aerosol delivery devices (ISO 20072).
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