STN EN ISO 20186-3
Name: | STN EN ISO 20186-3 |
Validity: | Valid |
Number of pages: | 28 |
Language: |
EN
|
Paper: | 14,10€ |
Electronic version |
a) Only read (without ability to print and copy)
12,69€ b) Without ability to print, with ability to copy (printscreen) 14,10€ c) With ability to print and copy (printscreen) 18,33€ |
Slovak title | Molekulárno-diagnostické vyšetrenia in vitro. Špecifikácie postupov pred vyšetrením krvi. Časť 3: Izolovaná voľne cirkulujúca bunková DNA z plazmy (ISO 20186-3: 2019) |
English title | Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019) |
Release Date: | 01. 02. 2020 |
Date of withdrawal: | |
ICS: | 11.100.10 |
Sorting character/National clasification code | 85 1023 |
Level of incorporation: | idt EN ISO 20186-3:2019, idt ISO 20186-3:2019 |
Official Journal | 01/20 |
Amendments | |
Replaced by: | |
Repleces: | |
Note in Official Journal: | |
Subject of the standard: | This document provides recommendations and requirements on the handling, storage, processing and documentation of venous whole blood specimens intended for circulating cell free DNA (ccfDNA) examination during the pre-examination phase before an analytical test is performed. This document covers specimens collected in venous whole blood collection tubes. This document is applicable to any molecular in vitro diagnostic examination performed by medical laboratories. It is also intended to be used by laboratory customers, in vitro diagnostics developers and manufacturers, biobanks, institutions and commercial organizations performing biomedical research, and regulatory authorities. |
Preview: | Náhľad normy (PDF) |