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21 resultaten gevonden voor 'control procedure'

control procedure

set of operations at the point of use, described specifically, intended to monitor the performance characteristics of an IVD medical device and fulfil requirements for quality

Norm
NEN-EN-ISO 18113-1:2011 en
Titel
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
Paragraaf
3.14

procedure

specified way to carry out an activity or a process (3.1.9)

Norm
NEN-EN-ISO 14050:2020 en
Titel
Environmental management - Vocabulary
Paragraaf
3.3.6

procedure

specified way to carry out an activity or a process (3.36)

Norm
NEN-ISO 13065:2015 en
Titel
Sustainability criteria for bioenergy
Paragraaf
3.35

procedure

gespecificeerde manier om een activiteit of een proces uit te voeren (3.27)

Norm
ISO 20121:2012 nl
Titel
Duurzame evenementen - Managementsystemen - Eisen met richtlijnen voor gebruik
Paragraaf
3.28

procedure

specified way to carry out an activity or a process (3.4.1)

Norm
NEN-EN-ISO 9000:2015 en
Titel
Quality management systems - Fundamentals and vocabulary
Paragraaf
3.4.5

procedure

specified way to carry out an activity or a process

Norm
NEN-EN 16751:2016 en
Titel
Bio-based products - Sustainability criteria
Paragraaf
3.23

procedure

specified way to carry out an activity or a process (3.27)

Norm
ISO 20121:2012 en
Titel
Event sustainability management systems - Requirements with guidance for use
Paragraaf
3.28

measurement procedure

detailed description of a measurement according to one or more measurement principles and to a given measurement method, based on a measurement model and including any calculation necessary to obtain a measurement result

Norm
NEN-EN-ISO 18113-1:2011 en
Titel
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
Paragraaf
3.44

change control

<configuration management> activities for control of the output (3.7.5) after formal approval of its product configuration information (3.6.8)

Norm
NEN-EN-ISO 9000:2015 en
Titel
Quality management systems - Fundamentals and vocabulary
Paragraaf
3.3.10

control material

substance, material or article intended by its manufacturer to be used to verify the performance characteristics of an IVD medical device

Norm
NEN-EN-ISO 18113-1:2011 en
Titel
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
Paragraaf
3.13