EN 13640:2002

Stability testing of in vitro diagnostic reagents EN 13640:2002

Publication date:   Jan 22, 2004

General information

99.60 Withdrawal effective   Dec 1, 2011

CEN

CEN/TC 140 In vitro diagnostic medical devices

European Norm

11.100   Laboratory medicine

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Scope

This standard is applicable to the stability testing of in vitro diagnostic reagents including reagent products, calibrators, control materials and kits, hereinafter called IVD reagents. It specifies general requirements for stability testing and gives specific requirements for real-time testing and accelerated testing when generating stability data in the

- determination of IVD reagent shelf-life including transport stability;

- determination of stability of the IVD reagent in use after the first opening of the primary container (e. g. on-board stability);

- monitoring of stability of IVD reagents already placed on the market;

- verification of stability after IVD reagent modifications that may affect stability.

This standard does not apply to instruments, apparatus, equipment, systems, or specimen receptacles.

Related legislation

Legislation related to this standard

98/79/EC

In vitro diagnostic medical devices

Harmonized/Supporting

Life cycle

NOW

WITHDRAWN
EN 13640:2002
99.60 Withdrawal effective
Dec 1, 2011

REVISED BY

WITHDRAWN
EN ISO 23640:2011