90.60 Close of review Sep 2, 2025
CEN
CEN/TC 140 In vitro diagnostic medical devices
European Norm
11.100 Laboratory medicine
Published
This European Standard specifies sampling procedure requirements for acceptance testing of finished in vitro diagnostic medical devices, which require EU verification by a notified body.
Two different provisions are addressed:
a) verification by testing attributes and/or variables on a statistical basis;
b) verification by testing a homogeneous batch which has been defined by appropriate means of process validation and in-process control.
This standard specifies requirements and criteria for testing procedures to establish and verify the homogeneity of processes and products. This standard is also applicable for drawing up sampling plans for finished products according to the requirements laid down for manufacturers' product certification and production quality systems.
Legislation related to this standard
In vitro diagnostic medical devices
Harmonised Standard / Cited in the Official Journal
PUBLISHED
EN 13975:2003
90.60
Close of review
Sep 2, 2025