ISO 17025:2017 Awareness Training

Traibcert Awareness online course is a comprehensive package that delves into every nook and corner you deserve to know about ISO 17025, including all the erstwhile requirements and pragmatic impeccability for compliance. The course is durably defined for novices who exhibit great affinity towards testing and calibration management and ISO standards.

Instructor: Mr Kumaravel

Language: English

Validity Period: 365 days

$269 22% OFF

Course Objective

The well-documented training resources, organized agendas, planning and outlay materials that have been fastidiously constructed, precisely moulded and systematically presented, have been laboriously authorized by qualified experts in the exclusive domain of advanced tertiary education. The anticipated objective of both the tutors and pedagogues is to pre-dominantly provide the authorized staff with the essential basic knowledge/experience in the ingenuity of ISO 17025 – LMS and to concurrently spawn a suitable platform to fulfil the implementation process, vesting the staff who are conferred with loftier understanding of the management systems approach and the requirements of ISO 17025, consequently affording requisite tools for teams/groups/panels preparing for implementation.

Who can attend the Course

The course is designed to suit all who are interested to play a significant role in the Laboratory management system and for those who are responsible for internal management system audits including Laboratory head, department managers, supervisors, Laboratory technician, Team leader, representatives, engineers, and administrative staff that have a focus on Testing and calibration improved performance and profitability.

Prerequisite

This course is exclusively formulated for beginners and for group training sessions in organizations to develop the quality testing and calibration intrinsic culture of the meritorious programme.

No prior knowledge is needed to take the course.
We recommend that participants have previous knowledge of the following to maximize the course benefits.
This course is uniquely designed for students/Teams/ laboratory heads who possess an existing knowledge of, or experience in, laboratory management. It provides an overview of the management systems approach and the requirements of ISO 17025.
It can be used as a foundation for those who have developed an insistent urge to complete a certified auditor/ management system auditor training courses.

Course Duration

The course duration is approximately 16 hrs

Final Assessment - 40 mins.

Materials provided during the tenure of the course (video lectures, all-inclusive erudite articles and probing activities) are the essential ingredients absolutely compulsory to efficaciously achieve the certification Assessment

Key Session

Topic	Duration
Module 1 - Introduction about ISO 17025:2017 and process approach	33 min
Module 2 - Laboratory Management System Principles	45 min
Module 3 - Overview of Clause 1-3	42 min
Module 4 - General Requirements	27 min
Module 5 - Structural Requirements	69 min
Module 6 - Resource Requirements	135 min
Module 7 - Process Requirements	243 min
Module 8 - Management System Requirements	102 min
Module 9 - Internal Audit Module ISO 19011:2018	210 min
Final assessment	40 min

Reviews

Load More Reviews

Other Courses


	Module 1 - Introduction about ISO 17025:2017 and process approach
		Introduction to ISO 17025 Awareness training
		Objectives of the Course
		Scope of training
		About ISO
		General requirements of ISO 17025
		Reminder of principles
		Applying Principles
	Module 2 - Laboratory Management System Principles
		Main changes in approach Vs 17025
		Main changes in approach Vs 17025
		Main changes in approach Vs 17025
		Comparison of 2005 & 2017
		Why Restructure 17025
		Management System Options
		The New Structure
		Headlines of changes
		Other Changes
		ISO 17025 Timeline
		Introduction steps to accreditation
		ISO 17025 Applicability
		ISO 17025 Accreditation benefits
		Benefits- ISO 17025
		Overview of Requirements
	Module 3 - Overview of Clause 1-3
		10 steps to implementation of ISO 17025
		ISO/IEC 17025 comparison clause regroup
		Main changes compared to 2005
		Introduction to ISO 17025:2017
		Overview of Clause
		1.0 Scope
		2.0 Normative Ref
		3.0 terms and definition
		3.0 terms and definition
		3.0 terms and definition
	Module 4 - General Requirements
		4.0 General Requirements
		Clause 4.1 Impartiality (4.1.1 - 4.1.3)
		Clause 4.1 Impartiality (4.1.4 - 4.1.5)
		4.2 Confidentiality 4.2.1
		4.2 Confidentiality 4.2.2
		4.2 Confidentiality 4.2.3 & 4.2.4
	Module 5 - Structural Requirements
		5.0 Structural requirements
		5.0 Structural requirements (5.1 & 5.2)
		5.0 Structural requirements 5.3
		5.0 Structural requirements 5.4
		5.0 Structural requirements 5.5
		5.0 Structural requirements 5.6
		5.0 Structural requirements 5.7
		Clause 4.0 & 5.0 Summary
		Assignment -1- ISO 17025 AW
		Section Quiz 4 & 5
	Module 6 - Resource Requirements
		6.0 Resource requirements
		6.1 General
		6.2 Personnel 6.2.1 & 6.2.2
		6.2 Personnel 6.2.3 & 6.2.4
		6.2 Personnel 6.2.5 & 6.2.6
		6.3 facilities and environmental conditions 6.3.1, 6.3.2 & 6.3.3
		6.3 Facilities and environmental conditions 6.3.4 & 6.3.5
		6.4 Equipment 6.4.1 & 6.4.2
		6.4 Equipment 6.4.3 & 6.4.4
		6.4 Equipment 6.4.5 & 6.4.6
		6.4 Equipment 6.4.7 & 6.4.8
		6.4 Equipment 6.4.9
		6.4 Equipment 6.4.10, 6.4.11 & 6.4.12
		6.4 Equipment 6.4.13
		6.5 Metrological traceability 6.5.1 & 6.5.2
		6.5 Metrological traceability 6.5.3
		6.6 Externally Provided Products and services 6.6.1
		6.6 Externally Provided Products and services 6.6.2 & 6.6.3
		Clause 6.0 Summary
		Assignment -2- ISO 17025 AW
		Section Quiz 6
	Module 7 - Process Requirements
		7.0 Process Requirements
		7.1 Review of requests, tenders and contracts 7.1.1 & 7.1.2
		7.1 Review of requests, tenders and contracts 7.1.3 & 7.1.4
		7.1 Review of requests, tenders and contracts 7.1.5 & 7.1.6
		7.1 Review of requests, tenders and contracts 7.1.7 & 7.1.8
		7.2 Selection, verification and validation of methods 7.2.1
		7.2 Selection, verification and validation of methods 7.2.1
		7.2 Selection, verification and validation of methods 7.2.1
		7.2 Selection, verification and validation of methods 7.2.1
		7.2.2 Validation of methods
		7.2.2 Validation of methods
		7.2.2 Validation of methods
		7.3 Sampling 7.3.1 & 7.3.2
		7.3 Sampling 7.3.3
		7.4 Handling of test or calibration items 7.4.1 & 7.4.2
		7.4 Handling of test or calibration items 7.4.3 & 7.4.4
		7.5 Technical records 7.5.1 & 7.5.2
		7.6 Evaluation of measurement uncertainty 7.6.1 & 7.6.2
		7.6 Evaluation of measurement uncertainty 7.6.3
		7.7 Ensuring the validity of results 7.7.1
		7.7 Ensuring the validity of results 7.7.2 & 7.7.3
		7.8 Reporting of results 7.8.1 General
		7.8 Reporting of results 7.8.2 Common requirements for reports
		7.8 Reporting of results 7.8.2 Common requirements for reports
		7.8.3 Specific requirements for test reports
		7.8.4 Specific requirements for calibration certificates 7.8.4.1
		7.8.5 Reporting sampling - specific requirements
		7.8.6 Reporting statements of conformity
		7.8.7 Reporting opinions and interpretations
		7.8.8 Amendments to reports
		7.9 Complaints 7.9.1 & 7.9.2
		7.9 Complaints 7.9.3, 7.9.4 & 7.9.5
		7.9 Complaints 7.9.6 & 7.9.7
		7.10 Nonconforming work 7.10.1
		7.10 Nonconforming work 7.10.2 & 7.10.3
		7.11 Control of data and information management
		7.11 Control of data and information management
		7.11 Control of data and information management
		Clause 7.0 Summary
		Assignment -3- ISO 17025
		Section Quiz 7
	Module 8 - Management System Requirements
		8.0 Management system requirements
		8.1 Options 8.1.1 General 8.1.2 Option A
		8.2 Management System documentation (Option A)
		8.2 Management System documentation (Option A)
		8.3 Control of Management System documentations (Option A)
		8.4 Control of records (Option A)
		8.5 Actions to address risks and opportunities (Option A)
		8.5 Actions to address risks and opportunities (Option A)
		8.6 Improvement (Option A)
		8.7 Corrective actions (Option A)
		8.8 Internal Audits (Option A)
		8.9 Management reviews (Option A)
		8.9 Management reviews (Option A)
		RECAP
		Thank you
		Section Quiz 8
	Module 9 - Intenal Audit Module ISO 19011:2018
		Introduction to ISO 19011- Internal audit
		Audit definition
		Audit Terms and Definitions
		Principles of Auditing
		Principles of Auditing
		Audit Objectives
		Internal Vs External Audits
		Planning and preparation of audit - different stages in an audit cycle
		Audit Management
		Internal Audits
		Planning and preparation for an audit
		Planning and preparation of audit
		Planning and preparation for an audit- Initiating the audit
		Audit criteria Vs audit scope
		Planning & Preparation of an Audit Selection of an audit team
		Planning & Preparation of an Audit - Document review
		Planning & Preparation for an Audit Preparation for on-site audit
		Performing an audit- Audit Management
		Performance of an Audit
		Performing an Audit – From collecting information to audit conclusions
		Audit team - Participants
		Key qualities of an auditor
		Performing an Audit – Audit Approach – Attitude of Auditor
		Audit approach - Communication process
		Audit approach - Communication process
		Audit approach - Communication process
		Audit approach - Communication process
		Audit approach - Communication process
		Audit approach - Communication process
		Audit approach - Communication process
		Audit Approach – Questioning techniques
		Audit Approach – Questioning techniques
		Audit approach - Communication process- clarifying questions
		Documentary evidence and follow up actions
		Performing an Audit – How do auditors find evidence ?
		Time management - Preparing a Checklist Format
		Preparing a Checklist Format
		Purpose of checklists
		Visit the field – Move around
		Performing an Audit -Observe Operational Control
		Performing an Audit -Observe Operational Control
		Section Quiz IQA
		Follow Audit trials
		Audit Management - reporting an audit
		Audit reporting
		Audit reporting – Writing Non-conformity reports
		NCR’s & Corrective actions Concepts relating to requirements
		Audit reporting – Writing Non-conformity reports
		NCR’s and Corrective actions -Examples of Objective Evidence
		Audit reporting – Writing Non-conformity reports
		Audit reporting – Writing Non-conformity reports
		NCR’s and Corrective action
		Writing Non-conformity reports Do and donts
		Writing Non-conformity reports- scenario- 1
		Writing Non-conformity reports- scenario- 2
		Writing Non-conformity reports- matrix
		Writing Non-conformity reports- auditor and auditee
		Writing Non-conformity reports- corrective action
		Difficulties encountered during internal audits
		A piece of counsel
		THANK you
	Final assessment - ISO 17025:2017 Awareness Training
		Final Assessment ISO 17025

Sign Up Complete your profile

Log In

You may also be interested in