C-01
ISO/IEC 17025 awareness
What the standard actually requires of a laboratory, in plain language, for teams who have to work to it rather than write it.
TRAINING / C-01
In detail
For laboratory staff, quality teams and managers who have to operate inside ISO/IEC 17025 without having read all of it.
Who it is for
01 / 03Analysts and technicians who follow the system daily, quality staff who maintain it, and managers who are accountable for it. No prior knowledge of the standard is assumed.
It is also useful for organisations preparing to seek accreditation for the first time, where the most common failure is not technical competence but not understanding what evidence the assessor will ask to see.
What is covered
02 / 03The structure of the standard and what each clause is actually asking for. Impartiality and confidentiality as operating requirements rather than statements. Personnel competence and how it is evidenced. Equipment, traceability and calibration. Method selection and validation. Handling of items. Reporting of results, including decision rules and statements of conformity.
The session is built around real records rather than slides of clause numbers. Most of the day is spent looking at what good and bad evidence actually looks like.
What you leave with
03 / 03An understanding of which clauses generate the findings that actually get raised, what an assessor is looking for when they ask a question, and where your own system is most likely to be thin.
At a glance
- Duration
- 1 day
- Delivered
- On site or at the laboratory
- Language
- English or Arabic
- Certificate
- Attendance certificate issued
Requests are read at the bench.
Send the sample question or the instrument list. It is read by a bench professional, not routed through a ticket queue. Confirmed phone, mailbox and address publish here at launch.