Mastering ISO/IEC 17025: 2017 and Certified Internal Auditor

Name: Mastering ISO/IEC 17025: 2017 and Certified Internal Auditor
Rating: 4.6 (212 reviews)

Detailed understanding of ISO/IEC 17025-2017 standard and that for conducting an effective internal audit.

Highest Rated

Created bySubhasis Mallik

Last updated 1/2021

English

What you'll learn

Detailed understanding of the clauses of ISO/IEC 17025 - 2017 standard.
How to implement ISO/IEC 17025 requirements in a test or calibration laboratory.
Skill for auditing laboratory activities for ISO/IEC 17025 - 2017.
Preparation of laboratory documents such as quality manual, system procedure etc.

Course content

15 sections • 55 lectures • 21h 55m total length

Introduction and content12:42
Know the objective and coverage of this course to decide its suitability for you.
What is quality management system (QMS) and QMS audit?6:53
A basic understanding of quality management system (QMS) and QMS audit.
General information about laboratory accreditation.28:31
General understanding about laboratory accreditation process.
General information about laboratory accreditation.

6 Resource requirements.2:38
Description of different types of resources that are needed in laboratory.
6.1 Resource requirements - General.5:43
This section describes the general resource requirements.
6.2 Resource requirements - Personnel.18:26
This section explains the requirements for clause 6.2 personnel resources for understanding, implementation and auditing perspective.
6.3 Resource requirements - Facility and environmental conditions.15:19
This section explains the requirements for clause 6.3 Facility and environmental conditions resources for understanding, implementation and auditing perspective.
6.4 Resource requirements - Equipment.1:18:10
This section explains the requirements for clause 6.4 Equipment resources for understanding, implementation and auditing perspective.
6.5 Resource requirements - Metrological traceability.46:19
6.6 Resource requirements - Externally provided products and services.31:23
This section explains the requirements for clause 6.6 Externally provided product and services resources for understanding, implementation and auditing perspective.
6. Resource requirements.

7 Process requirements.2:55
List of subsections in Process requirements.
7.1 Process requirements - Review of request, tender and contract.23:48
This section explains the requirements for clause 7.1 Review of request, tender and contracts (Process requirement) for understanding, implementation and auditing perspective.
7.2.1 Process Requirements - Selection and verification of methods.16:23
This section explains the requirements for clause 7.2.1 Selection and verification of methods (Process requirement) for understanding, implementation and auditing perspective.
7.2.2 Process Requirements - Validation of methods.36:19
This section explains the requirements for clause 7.2.2 Validation of methods (Process requirement) for understanding, implementation and auditing perspective.
7.3 Process Requirements - Sampling.14:55
This section explains the requirements for clause 7.3 Sampling (Process requirement) for understanding, implementation and auditing perspective.
7.4 Resource Requirements - Handling of test or calibration items.19:20
This section explains the requirements for clause 7.4 Handling of test or calibration items (Process requirement) for understanding, implementation and auditing perspective.
7.5 Process Requirements - Technical records.15:43
This section explains the requirements for clause 7.5 Technical records (Process requirement) for understanding, implementation and auditing perspective.
7.6 Process Requirements - Evaluation of measurement uncertainty..38:26
This section explains the requirements for clause 7.6 Evaluation of measurement uncertainty (Process requirement) for understanding, implementation and auditing perspective.
7.7 Process Requirements - Ensuring validity of results.29:04
This section explains the requirements for clause 7.7 Ensuring validity of results (Process requirement) for understanding, implementation and auditing perspective.
7.8 Process Requirements - Reporting of results.1:39:47
This section explains the requirements for clause 7.8 Reporting of results (Process requirement) for understanding, implementation and auditing perspective.
7.9 Process Requirements - Complaints.11:31
This section explains the requirements for clause 7.9 Complaints (Process requirement) for understanding, implementation and auditing perspective.
7.10 Process Requirements - Non-conforming work.11:02
This section explains the requirements for clause 7.10 Non-conforming work (Process requirement) for understanding, implementation and auditing perspective.
7.11 Process Requirements - Control of data and information management.15:59
This section explains the requirements for clause 7.11 Control of data and information management (Process requirement) for understanding, implementation and auditing perspective.
7. Process requirements.

8.1 Management System Requirements - General.9:16
This section explains the requirements for clause 8.1 Management system requirement - General requirements for understanding, implementation and auditing perspective.
8.2 Option-A - Management system documentation.17:56
This section explains the requirements for clause 8.2 Option-A, Management system documentation for understanding, implementation and auditing perspective.
8.3 Option-A - Control of management system documents.11:30
This section explains the requirements for clause 8.3 Option-A, Control of management system documents for understanding, implementation and auditing perspective.
8.4 Option-A - Control of records.12:33
This section explains the requirements for clause 8.4 Option-A, Control of records for understanding, implementation and auditing perspective.
8.5 Option-A - Actions to address risk and opportunities.20:38
This section explains the requirements for clause 8.5 Option-A, Action to address risk and opportunities for understanding, implementation and auditing perspective.
8.6 Option-A - Improvement.8:24
This section explains the requirements for clause 8.6 Option-A, Improvements for understanding, implementation and auditing perspective.
8.7 Option-A - Corrective action.24:08
This section explains the requirements for clause 8.7 Option-A, Corrective action for understanding, implementation and auditing perspective.
8.8 Internal audit.17:39
This section explains the requirements for clause 8.8 Option-A, Internal audit for understanding, implementation and auditing perspective.
8.9 Management review.13:21
This section explains the requirements for clause 8.9 Option-A, Management review for understanding, implementation and auditing perspective.
8. Management system requirements.

Internal Audit Guideline (ISO 19011: 2018) General understanding of QMS audit20:12
This section describes the general understanding about QMS audit.
Internal Audit Guideline (ISO 19011) Phase-1: Audit planning and preparation6:13
This section explains the Phase-1 of QMS Audit which is planning and preparation.
Internal Audit Guideline (ISO 19011) Phase-2: Performing the audit35:49
This section explains the Phase-2 of QMS Audit which is performing the audit.
Internal Audit Guideline (ISO 19011) Phase-3: Reporting of audit29:51
This section explains the Phase-3 of QMS Audit which is reporting of audit.
Internal Audit Guideline, Phase-4: Correction, corrective action and follow up23:47
This section explains the Phase-4 of QMS Audit which is correction, corrective action and follow up.
Internal audit.

Requirements

Must be familiar with test or calibration laboratory.
A degree / diploma is science / engineering / technology / management is desired, but not a key factor.
Keen to practice quality management system in testing or calibration laboratory.

Description

This course is intended for providing detailed knowledge and practical understanding about the auditable clauses of ISO/IEC 17025-2017 standard (General requirements for the competence of testing and calibration laboratories). This covers the general understanding of laboratory accreditation process and detailed explanation of all clauses of the standard. Apart from that understanding of audit process for this standard is also covered in details. Some of the hot spot activities of laboratory accreditation process are explained with additional elaborations, e.g. intermediate check, metrological traceability, method validation, measurement uncertainty, decision rule, root cause analysis, risk and opportunity assessment etc. Specific guidance is provided for preparation of system documents, such as quality manual, system procedure. The various important aspects of requirements of accreditation agency are also elaborated. Several quizzes are added in the course which would help participant to check their understanding of the topics covered in video lecture. Very useful downloadable materials are provided so that the users can apply these in their application such as internal audit and also gain technical knowledge. The full content of ISO/IEC 17025-2017 standard is mentioned in the audit checklist which would be a very useful reference for laboratory practitioners. At the end an assignment is added for evaluation purpose for issue of certificate which would recognize the participant as a certified internal auditor for this standard.

Who this course is for:

Freshers from college looking for a career in testing or calibration laboratory.
Working executives of testing and calibration laboratory.
Top management and section in-charges of testing and calibration laboratory.
Quality manager of test or calibration laboratory.
Individual providing consultancy for laboratory accreditation.

Mastering ISO/IEC 17025: 2017 and Certified Internal Auditor

What you'll learn

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Course content

Introduction, content and general information3 lectures • 48min

Clauses of ISO/IEC 17025-2017 and Steps for Laboratory accreditation.1 lecture • 31min

Clause 4: General requirements.1 lecture • 30min

Clause 5: Structural Requirements1 lecture • 1hr 3min

Clause 6: Resource requirements.7 lectures • 3hr 18min

Clause 7: Process Requirements13 lectures • 5hr 35min

Clause 8: Management system requirements.9 lectures • 2hr 15min

Risk and opportunity assessment1 lecture • 35min

QMS Audit Guideline (ISO 19011-2018)5 lectures • 1hr 56min

Documentation of Quality Manual and Quality System Procedure1 lecture • 1hr 15min

Requirements

Description

Who this course is for: