Skip to main content
Back

ISO 20391-1:2018

Biotechnology -- Cell counting -- Part 1: General guidance on cell counting methods

General information

Valid from 19.01.2018
Directives or regulations
None

Standard history

Status
Date
Type
Name
19.01.2018
Main
ISO 20391-1:2018 defines terms related to cell counting for biotechnology. It describes counting of cells in suspension (generally cell concentration) and cells adhered to a substrate (generally area density of cells). It provides key considerations for general counting methods (including total and differential counting, and direct and indirect counting) as well as for method selection, measurement process, and data analysis and reporting.
ISO 20391-1:2018 is applicable to the counting of all cell types ? mammalian and non-mammalian (e.g. bacteria, yeast) cells.
ISO 20391-1:2018 is not intended for counting of cells while in a tissue section or a biomaterial matrix.
Several sector/application-specific international and national standards for cell counting currently exist. When applicable, the user can consult existing standards when operating within their scope (specific measurement techniques and/or applications).

Required fields are indicated with *

*
*
*
PDF
133.39 € incl tax
Paper
133.39 € incl tax
Standard monitoring

Customers who bought this item also bought

Main

EVS-EN ISO 14971:2019

Medical devices - Application of risk management to medical devices (ISO 14971:2019)
Valid from 02.01.2020
Main

EVS-EN ISO 18113-1:2011

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
Withdrawn from 15.07.2024
Main

EVS-EN ISO 18113-2:2011

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
Withdrawn from 01.07.2024
Main

EVS-EN ISO 18113-3:2011

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
Withdrawn from 01.07.2024