Training | Consultancy | Auditing 
+353 1 204 0646 
Hello guest
Your basket is empty

Internal Auditor ISO 13485:2016 - 2 Days -  Virtual Classroom 

IRCA Certified ISO Internal Auditor Training Nov 11 & 12 2021 

€549  Price includes training, all training materials, pre-course study materials, IRCA registration, refreshments during the training where applicable.  Need a quote for In-house Training email us today 

IQC Are One of only Two CQI_IRCA approved trainers for ISO 13485:2016 Internal Auditor. 
It is essential for modern organisations to have Management Systems in place and to effectively audit them in a way that’s organised, systematic and that also adds value. 
This course will assist auditors, particularly those who audit internally against any standard, (for example ISO13485 and cGMP to do so from a process-based perspective to check for Effectiveness, Conformance and identify Improvement opportunities. This programme is applicable to both the private and public sector. 
Who should attend? 
Internal auditors. 
Quality Managers and those with internal auditing / self inspection responsibilities across all departments. 
Senior Departmental Management and Area/Process Owners. 
Those who want to pursue a career as an Auditor/Lead Auditor. 
Anyone responsible for or aspiring to conduct internal QEHS Management System audits. 
Please note that participants attending the internal Auditor course are expected to have some prior knowledge of quality management principles and concepts, and the basic requirements of the relevant QMS standard. 
IQC will provide a “Pre-course” pack to all delegates approximately 10 days before the training commences, however, if you are new to ISO 13485 please consider one of our Fundamental and Foundation training courses. 
As places are limited, book early to avoid disappointment. 
Places cancelled within 10 working days of commencement must be paid in full. Substitutions may be made at any time at no additional charge. 
Course Objectives 
Describe the purpose of a quality management system in relation to ISO 13485. 
Understand the structure and key requirements of ISO standards and regulations. 
Interpret requirements of standards and regulations in the context of an audit. 
Describe the role of the internal audit in the maintenance and improvement of management systems. 
Understand the different types of audits. 
Describe the roles and responsibilities of auditors and lead auditors. 
Plan and conduct an audit in accordance with ISO 19011, demonstrating ability to plan and prepare effectively 
Gather objective evidence, through effective interviewing, observation, sampling and note taking. 
Analyse and interpret information in order to determine conformance with requirements, effectiveness, and areas for improvement. 
Report the audit, including writing valid, factual and value-adding audit reports 
Undertake audit follow-up activities, including evaluating the effectiveness of corrective actions. 
Professionally liaise with external auditors.During the two days participants will acquire knowledge and skills in auditing. However, auditing like any other acquired skill requires practice. The best place to practice and extend your experience is during actual audits. 
Day 1 (summary) 
Management Systems & Quality Management Systems - Plan-Do-Check-Act cycle 
Structure of ISO standards for example ISO 13485 
Understanding process management 
Audit objectives - Auditing conformance, effectiveness and improvement  
Scheduling of the audit programme on key processes and not areas of the Standard 
Audit preparation – understanding the organisation and its key processes 
Checklists, Audit plans, Productive meetings (Opening Meetings) 
Day 2 (summary) 
Carrying out the audit… 
Teamwork, Collecting information, Communications 
Human behaviour, Audit sampling, Audit findings 
Evaluating the effectiveness of the Quality System in addition to conformance audits 
Opening and Closing Meetings 
Virtual / Live Audit - Participants put into practice what they learned on Days 1 and 2. 
Writing the audit report - Taking corrective action - Management of the audit programme. 
Internal Auditor ISO 13485 | 4 and 5 Nov 2021
The only CQI_IRCA approved ISO 13485:2016 Internal Auditor training in Ireland. Training – 2 Day Course
This programme is applicable to auditors and support auditors in the Medical Device Industry.
If you are purchasing the course on behalf of a colleague please fill in the details below so we can email important course material. If there are additional attendees please add their details in the Additional Attendee section at checkout.
Delegate 1: Name of Delegate:
Delegate 1:Personal Email (work email blocks training materials):
Delegate 1: Personal Mobile Number (to directly contact you):
Add Another Delegate(s):
Payment options include:
Bank Transfer
Purchase Order
Credit Card
Our site uses cookies. For more information, see our cookie policy. Accept cookies and close
Reject cookies Manage settings