The International Standard Organization (ISO / IEC) announced in November 2017 that the new requirements for the competence of testing and calibration laboratories transition period would be until November 30, 2020. At the end of the transition period, they will base the laboratory’s accreditation on ISO/IEC 17025:2017.
Due to the COVID-19 pandemic, the International Laboratory Accreditation Cooperation (ILAC) has extended the transition period globally to June 1, 2021.
What is the ISO/IEC 17025 Standard?
The ISO/IEC 17025 standard stipulates the requirements for the competence of testing and calibration laboratories. The requirements are pertinent to all organizations performing testing, sampling, and calibrations. ISO/IEC 17025 is the highest quality management system and is recognized as the global quality control standard.
Before the ISO/IEC 17025:2017, the international standard was ISO/IEC 17025:2005. They review the standards every five years to update and modernize practices when needed. There are several differences between the two. Here is what changed:
ISO/IEC 17025:2005
The 2005 version included scope, normative references, terms and definitions, management, and technical requirements.
ISO/IEC 17025:2017
The 2017 version includes scope, normative references, terms and definitions, general requirements, structural requirements, resource requirements, process requirements, and management system requirements.
The terminology has been updated, and these modifications are also in the International Vocabulary of Metrology (VIM).
The newest standard emphasizes information technology. Specifically in the use of systems, provision of electronic test results, and the provision of electronic records.
Specific on the Changes
Each category mentioned above has additions and changes that each maintains.
• Scope: The revisions in the scope category apply to testing, calibration, and sampling.
• Structure: A new structure is applied to align the standard with other existing conformity standards. One of these is the conformity assessment.
• Process Approach: It updates the process approach to be similar to ISO 9001 (quality management), ISO 15189 (quality of medical laboratories), and ISO/IEC 17012-1 (requirements for audit and certification bodies).
• Terminology: An update in terminology and addition of phrases such as “laboratory” with clear definitions.
• Risk-Based Thinking: The new concept ensures that risks are identifiable, considered, and monitored throughout the design and quality management system. There are commonalities with ISO 9001:2015.
How do These Changes Benefit Accredited Labs?
One of the most significant benefits a calibration lab will gain is international recognition for its commitment to quality, competency, and reliable results. It is a way to assure customers that you have the technical competence to get their instruments done accurately. Ultimately, it is guaranteed that your lab is performing at the highest level.
Looking for a Calibration Lab?
Finding an ISO/IEC 17025:2017 accredited lab for laboratories seeking calibration labs means you are working with the best. The new standards will ensure that the test results, reports, and records are compliant and that the instrumentation will perform to its ideals. Do your due diligence and research calibration labs that understand the importance of exceptional service, which you can find at SRP control systems Ltd.
