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Professional Leadership Development Quality Management Systems - Laboratories Certificate in ISO 17025

COURSE OVERVIEW: This course caters for candidates with diverse industry backgrounds, wanting to implement positive outcomes for organisations having "Laboratories" as well as training them to be able to confidently and professionally conduct evaluations and or audits on an Organisations Business Processes to ISO 17025 Compliance.

The candidate will be involved in carrying out an Audit on either a newly established Quality Management System or within an established system thoroughly checking and auditing existing laboratory documentation plus all of the organisations Management Programmes. By the completion of this course the candidate will have ensured that the business system in place has been implemented and audited correctly and the organisation is ready for preparation for a Third Party Audit (Certification Audit). Participants will also be able to undertake a full Skill Examination online to ready them for RABQSA Auditor Certification if they choose.

COURSE PRICE: $800.00 AUD

COURSE RECOGNITION: Certificate of Competence ACI-LB, RABQSA-QM & RABQSA-AU.

COURSE LENGTH: Dependent on Candidates and or organisational time commitments and resources.

COURSE APPROVAL NUMBERS: ACI-LB, RABQSA-QM and RABQSA-AU.

COURSE CODE: QMSIALAB

COURSE FACILITATOR: RABQSA approved and appointed at course registration.

REFUND POLICY: - No refund upon completion of registration and enrollment process.

3 YEAR PROFESSIONAL DEVELOPMENT GUARANTEE: Each ACI Global Course or Programme is backed by a "3 Year Professional Leadership Development Guarantee" ensuring the Candidates Professional Leadership Development is maintained relevant to the training provided. This service is included in the Course or Programme Price and conditions apply.

The Key Learning Objectives covered in this course are:

• KEY LEARNING OBJECTIVE 1 - International Standards covered ISO 17025, ISO 9001, 9004, 19011 and 17021.
• KEY LEARNING OBJECTIVE 2 - Relevant Legislation, Statutory Laws and the Eight Quality Management Principles.
• KEY LEARNING OBJECTIVE 3 - Key Quality Policies, Objectives, Impacts and Key Performance Indicators (KPI's).
• KEY LEARNING OBJECTIVE 4 - Evaluating to ensure compliance to both ISO 17025 and ISO 9001:2008.
• KEY LEARNING OBJECTIVE 5 - Evaluating the developed QMS and its Laboratory documents and related records.
• KEY LEARNING OBJECTIVE 6 - Audit Definitions, Principles and Categories.
• KEY LEARNING OBJECTIVE 7 - Audit Sampling, Calibration's, Tracability.
• KEY LEARNING OBJECTIVE 8 - Stages of an Audit and followup activities.

The Key Learning Outcomes achieved with this course are:

KEY LEARNING OUTCOME 1 - Perform an Audit.

KEY LEARNING OUTCOME 2 - Achieve Competence in ISO 17025 and Quality Management Systems in line with the following Key Evidence Criteria:

• The Intent & Requirement of each clause of ISO 17025 and 9001 is Understood.
• The Relationship between the 8 QMP and ISO 17025 and 9001 is understood.
• Mandatory Documents required by ISO 17025 and 9001 is understood.
• Conformity to the clauses of ISO 17025 and 9001 is understood.
• Sub Contractor quality systems are evaluated.
• Equipment maintenance and control is evaluated and understood.
• Calibration techniques are evaluated and understood.
• Traceability techniques are evaluated and understood.
• Test procedures are evaluated and understood.
• Sample preparation and Non Standard Sampling Techniques are evaluated and understood.
• Environmental Conditions are evaluated and understood.
• The Audit Report used uses correct terminology.
• The Effectiveness of the QMS is evaluated.
• The Audit Report reflects the specific Business under audit.
• Difference between Legal Compliance and Conformity to ISO is reported.
• Product Realization Processes are Evaluated.
• Audit Evidence Demonstrates Conformance.

KEY LEARNING OUTCOME 3 - Achieve Competence in Auditing in line with the following Key Evidence Criteria:

• Audit Principles understood and applied.
• Audit Definitions understood and applied.
• Audit Criteria understood and applied.
• Audit Planning understood and applied.
• Document Review understood and applied.
• Onsite Audit Activities understood and applied.
• Audit Reporting understood and applied.
• Audit Evidence understood and evaluated.
• Followup Activities understood and applied.
• The Management System is audited to Criteria, Plan and Reference Standard.
• Sampling understood and applied.
• Techniques to establish positive relationships.
• "Attitude" - Cultural, Language and Ethical Issues.
• Regulations, Legal Requirements and Codes of Practice.
• Effective Communications understood and practiced.
• Personal Attributes and Questioning Techniques understood and practiced.

COURSE OR PROGRAMME ENROLLMENT: Getting started is as easy as clicking on the e-learning Registration Tab below, Register and Pay for your course all online and you can be started in less than 6 Hrs (Dependant on International Time Zones and Clearance of Funds).

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