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BSI - BS EN 13975

Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects

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Organization: BSI
Publication Date: 28 March 2003
Status: active
Page Count: 16
ICS Code (In vitro diagnostic test systems): 11.100.10

Document History

BS EN 13975
March 28, 2003
Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects
A description is not available for this item.

References

This document references:
ISO 2859-2 - Sampling procedures for inspection by attributes — Part 2: Sampling plans indexed by limiting quality (LQ) for isolated lot inspection
Published by ISO on February 1, 2020
This document specifies an acceptance sampling system for inspection by attributes indexed by limiting quality (LQ). The sampling system is used for lots in isolation (isolated sequences of lots, an...
This document references:
ISO 2859-3 - Sampling procedures for inspection by attributes - Part 3: Skip-lot sampling procedures
Published by ISO on May 1, 2005
This part of ISO 2859 specifies generic skip-lot sampling procedures for acceptance inspection by attributes. The purpose of these procedures is to provide a way of reducing the inspection effort on...
This document references:
ISO 2859-1 - Sampling procedures for inspection by attributes — Part 1: Sampling schemes indexed by acceptance quality limit (AQL) for lot-by-lot inspection AMENDMENT 1
Published by ISO on June 15, 2011
This part of ISO 2859 specifies an acceptance sampling system for inspection by attributes. It is indexed in terms of the acceptance quality limit (AQL). Its purpose is to induce a supplier through...
This document references:
BS EN ISO 9000 - Quality management systems - Fundamentals and vocabulary
Published by BSI on September 30, 2015
A description is not available for this item.
This document references:
EN 375 - Information Supplied by the manufacturer with in Vitro Diagnostic Reagents for Professional Use
Published by CEN on January 1, 2001
A description is not available for this item.
This document references:
98/79/EC CORR - CORRIGENDUM to the European Parliament and of the Council on in Vitro Diagnostic Medical Devices
Published by EU on October 27, 1998
A description is not available for this item.
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