NF EN ISO 11608-7

NF EN ISO 11608-7

August 2017
Standard Current

Needle-based injection systems for medical use - Requirements and test methods - Part 7 : accessibility for persons with visual impairment

ISO 11608-7:2016 specifies particular requirements to make needle-based drug delivery systems or NIS (needle-based injection system) accessible for persons with visual impairments. It applies to devices intended for patient or caregiver administration of medicinal products to humans.It covers requirements to allow for safe and correct handling of the NIS, including labelling, packaging, and instructions for use. It also includes requirements for training programs, if applicable.It covers requirements for NIS that are claimed to be appropriate for use by persons with visual impairments.It does not address requirements for use of sharps containers by persons with visual impairments.Although specifically intended to apply to needle-based injection systems within the ISO 11608 series, ISO 11608-7:2016 can be applied to NIS outside the ISO 11608 series as well, if they might be used by persons with visual impairments.It is written to address the needs of persons with all levels of visual limitations, including low, moderate, or severe visual impairment; legal, functional, or total blindness; and colour vision deficiencies.Therefore, ISO 11608-7:2016 includes the requirement to provide information in visual formats that can be perceived and understood by people with moderate visual impairment and in non-visual formats (e.g. tactile or auditory) that can be perceived and understood by people with no useful vision.For simplicity's sake, this range is described in ISO 11608-7:2016 as addressing the needs of individuals with moderate visual impairment or blindness.

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Main informations

Collections

National standards and national normative documents

Publication date

August 2017

Number of pages

31 p.

Reference

NF EN ISO 11608-7

ICS Codes

11.040.20   Transfusion, infusion and injection equipment
11.040.25   Syringes, needles and catheters

Classification index

S93-020-7

Print number

2 - 01/09/2017

International kinship

European kinship

EN ISO 11608-7:2017
Sumary
Needle-based injection systems for medical use - Requirements and test methods - Part 7 : accessibility for persons with visual impairment

ISO 11608-7:2016 specifies particular requirements to make needle-based drug delivery systems or NIS (needle-based injection system) accessible for persons with visual impairments. It applies to devices intended for patient or caregiver administration of medicinal products to humans.

It covers requirements to allow for safe and correct handling of the NIS, including labelling, packaging, and instructions for use. It also includes requirements for training programs, if applicable.

It covers requirements for NIS that are claimed to be appropriate for use by persons with visual impairments.

It does not address requirements for use of sharps containers by persons with visual impairments.

Although specifically intended to apply to needle-based injection systems within the ISO 11608 series, ISO 11608-7:2016 can be applied to NIS outside the ISO 11608 series as well, if they might be used by persons with visual impairments.

It is written to address the needs of persons with all levels of visual limitations, including low, moderate, or severe visual impairment; legal, functional, or total blindness; and colour vision deficiencies.

Therefore, ISO 11608-7:2016 includes the requirement to provide information in visual formats that can be perceived and understood by people with moderate visual impairment and in non-visual formats (e.g. tactile or auditory) that can be perceived and understood by people with no useful vision.

For simplicity's sake, this range is described in ISO 11608-7:2016 as addressing the needs of individuals with moderate visual impairment or blindness.

Table of contents
  • 1 Domaine d'application
  • 2 Références normatives
  • 3 Termes et définitions
  • 4 Exigences
  • 5 Méthodes d'essai
  • 6 Rapport d'essai
  • 7 Informations fournies par le fabricant
  • Annexe A Mesure de la vision et de la déficience visuelle: vision fonctionnelle et acuité visuelle
  • Annexe B Document d'orientation pour l'élaboration d'un mode d'emploi destiné aux personnes malvoyantes
  • Annexe C Processus pour l'établissement d'une spécification, de méthodes d'essai et de la vérification en rapport avec 5.1
  • Bibliographie
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