Norm

NEN-EN 13975:2003 en

Steekproefprocedures voor gebruik bij de fabricage van In-vitro-diagnostische medische apparatuur - Statistische overwegingen

49,30

Over deze norm

Status Definitief
Aantal pagina's 12
Commissie In vitro diagnostica
Gepubliceerd op 01-04-2003
Taal Engels
This European Standard specifies sampling procedure requirements for acceptance testing of finished in vitro diagnostic medical devices, which require EC 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.

Details

ICS-code 11.100.10
Nederlandse titel Steekproefprocedures voor gebruik bij de fabricage van In-vitro-diagnostische medische apparatuur - Statistische overwegingen
Engelse titel Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects
Vervangt
Normatieve verwijzingen
  • 98/79/EG, In vitro diagnostica

Winkelwagen

Subtotaal:

Ga naar winkelwagen