International

 

18 

© ISO/IEC 2017 – All rights reserved

---

 

ISO/IEC 17025:2017(E)

7.11 Control of data and information management

7.11.1 

The  laboratory  shall  have  access  to  the  data  and  information  needed  to  perform  laboratory 

activities.

7.11.2 

The  laboratory  information  management  system(s)  used  for  the  collection,  processing, 

recording, reporting, storage or retrieval of data shall be validated for functionality, including the proper 

functioning  of  interfaces  within  the  laboratory  information  management  system(s)  by  the  laboratory 

before introduction. Whenever there are any changes,  including laboratory software configuration or 

modifications to commercial off-the-shelf software, they shall be authorized, documented and validated 

before implementation.

NOTE 1  In this document “laboratory information management system(s)” includes the management of data 

and information contained in both computerized and non-computerized systems. Some of the requirements can 

be more applicable to computerized systems than to non-computerized systems.

NOTE 2  Commercial off-the-shelf software in general use within its designed application range can be 

considered to be sufficiently validated.

7.11.3 

The laboratory information management system(s) shall:

a)  be protected from unauthorized access;

b)  be safeguarded against tampering and loss;

c)  be operated in an environment that complies with provider or laboratory specifications or, in the 

case of non-computerized systems, provides conditions which safeguard the accuracy of manual 

recording and transcription;

d)  be maintained in a manner that ensures the integrity of the data and information;

e)  include recording system failures and the appropriate immediate and corrective actions.

7.11.4 

When  a  laboratory  information  management  system  is  managed  and  maintained  off-site  or 

through an external provider, the laboratory shall ensure that the provider or operator of the system 

complies with all applicable requirements of this document.

7.11.5 

The  laboratory  shall  ensure  that  instructions,  manuals  and  reference  data  relevant  to  the 

laboratory information management system(s) are made readily available to personnel.