NF EN ISO 15189

NF EN ISO 15189

August 2007
Standard Cancelled

Medical laboratories - Particular requirements for quality and competence

ISO 15189:2007 specifies requirements for quality and competence particular to medical laboratories.ISO 15189:2007 is for use by medical laboratories in developing their quality management systems and assessing their own competence, and for use by accreditation bodies in confirming or recognising the competence of medical laboratories.

Main informations

Collections

National standards and national normative documents

Publication date

August 2007

Number of pages

51 p.

Reference

NF EN ISO 15189

ICS Codes

03.120.10   Quality management and quality assurance
11.100.01   Laboratory medicine in general

Classification index

S92-060

Print number

1 - 03/08/2007

International kinship

European kinship

EN ISO 15189:2007
Sumary
Medical laboratories - Particular requirements for quality and competence

ISO 15189:2007 specifies requirements for quality and competence particular to medical laboratories.

ISO 15189:2007 is for use by medical laboratories in developing their quality management systems and assessing their own competence, and for use by accreditation bodies in confirming or recognising the competence of medical laboratories.

Replaced standards (1)
NF EN ISO 15189
October 2003
Standard Cancelled
Medical laboratories - Particular requirements for quality and competence

Le présent document spécifie les exigences de qualité et de compétence propres aux laboratoires d'analyses de biologie médicale

Standard replaced by (1)
NF EN ISO 15189
December 2012
Standard Current
Medical laboratories - Requirements for quality and competence

ISO 15189:2012 specifies requirements for quality and competence in medical laboratories. ISO 15189:2012 can be used by medical laboratories in developing their quality management systems and assessing their own competence. It can also be used for confirming or recognizing the competence of medical laboratories by laboratory customers, regulating authorities and accreditation bodies.

ZOOM ON ... the Requirements department
To comply with a standard, you need to quickly understand its issues in order to determine its impact on your activity.

The Requirements department helps you quickly locate within the normative text:
- mandatory clauses to satisfy,
- non-essential but useful clauses to know, such as permissions and recommendations.

The identification of these types of clauses is based on the document “ISO / IEC Directives, Part 2 - Principles and rules of structure and drafting of ISO documents ”as well as on a constantly enriched list of verbal forms.

With Requirements, quickly access the main part of the normative text!

With Requirements, quickly access the main part of the normative text!
New: UPSELL service
- The UPSELL service allows you to easily update one of your standards.
- With a single click, add a new language, the Requirements or Redline+ service and add one or more additional users.
- Whether you are in the process of acquiring a standard or it is already available in your personal space, the UPSELL service is available at every stage to help you understand it and implement it within your organization.
Need to identify, monitor and decipher standards?

COBAZ is the simple and effective solution to meet the normative needs related to your activity, in France and abroad.

Available by subscription, CObaz is THE modular solution to compose according to your needs today and tomorrow. Quickly discover CObaz!

Request your free, no-obligation live demo

I discover COBAZ