SK EN ISO 23640:2017

Status: Published
Gjuha: English
Faqe: 13
Publikuar: 2017-12-01
Regjistri Kombëtar: 213/2017
Botim:

Standardet ndërkombëtare që kanë lidhje

This standard is identical to:
EN ISO 23640:2015
CEN/TC 140

Çmim: 18 €

Titulli Shqip

Pajisjet mjekësore për diagnostikimin in vitro -Vlerësimi i qëndrueshmërisë së reagentëve për diagnostikimin in vitro (ISO 23640 : 2011)

Titulli Anglisht

In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)

Scope Shqip

Asnjë informacion i shtuar.

Scope Anglisht

ISO 23640:2011 is applicable to the stability evaluation of in vitro diagnostic medical devices, including reagents, calibrators, control materials, diluents, buffers and reagent kits, hereinafter called IVD reagents. ISO 23640:2011 can also be applied to specimen collection devices that contain substances used to preserve samples or to initiate reactions for further processing of the sample in the collection device. ISO 23640:2011 specifies general requirements for stability evaluation and gives specific requirements for real time and accelerated stability evaluation when generating data in: the establishment of IVD reagent shelf life, including transport conditions suitable to ensure that product specifications are maintained; the establishment of stability of the IVD reagent in use after the first opening of the primary container; the monitoring of stability of IVD reagents already placed on the market; the verification of stability specifications after modifications of the IVD reagent that might affect stability.