Lead Auditor Training ISO 13485:2016

CQI & IRCA Certified Lead Auditor Training (ISO 13485:2016). Blended learning for quality professionals to audit QMS against ISO 13485. Gain an internationally recognized Lead Auditor certificate

Subsidised rate: €813    Full cost: €1,250

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Lead Auditor Training ISO 13485:2016


Level:ISO 13485:2016 Lead Auditor Certificate


Accredited by:IRCA


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Objectives

This CQI & IRCA Certified Blended ISO 13485:2016 Lead Auditor Course is ideal for anyone that wants to gain the knowledge and skills required to perform first, second and third-party audits of quality management systems against ISO 13485:2016, in accordance with ISO 19011 and ISO/IEC 17021

Content includes

Three learning objectives/outcomes:
 
At the end of this course, participants will be able to:
 
1. Explain the purpose of a quality management system, of quality management systems standards, of management system audit, of third-party certification and the business benefits of improved performance of the quality management system
2. Explain the role and responsibilities of an auditor to plan, conduct, report and follow-up a quality management system audit in accordance with ISO 19011, and ISO/IEC 17021, as applicable
3. Plan, conduct, report and follow-up an audit of a quality management system to establish conformity (or otherwise) with ISO 13485 and in accordance with ISO 19011, and ISO/IEC 17021, as applicable
 
Delivery:

This is a blended learning program, consisting of:

  • 16 hrs of online & self-paced modules (= 2 days training)
  • 3.5 virtual classroom days from 9am – 4.30pm
  • Examination held separately on day 4 from 10am – 12pm

Entry Criteria (Prior Learning Requirements)

In registering for this course, each Learner must have the following prior knowledge before completing this course:
Management Systems
• The Plan, Do, Check, Act (PDCA) Cycle
• The core elements of a management system and the interrelationship between top management responsibility, policy, objectives, planning, implementation, measurement, review and continual improvement.
ISO 13485
• Knowledge of the requirements of ISO 13485 and the commonly used quality management terms and definitions
• Knowledge of the requirements is a key pre-requisite in attending this course as without a good understanding, the course may be very challenging.

If any Learner does not meet the above entry criteria, successful completion of Comply Guru’s 10hr ISO 13485:2016 Requirements eLearning Course will ensure that they meet the above prior learning requirements.

For Quality Professionals or Engineers, Internal Auditors, Regulatory Professionals.

Qualification

Successful completion of this course will entitle each Participant to a CQI & IRCA Recognised ISO 13485:2016 Lead Auditor Certificate of Achievement.
Course accreditation held by Comply Guru (Course No. 2244)