QMS - Lead Auditor ISO: 13485:2016 - IRCA Certified

This programme is for those who wish to effectively audit a complete QMS (MD) based on the ISO 13485:2016 requirements with specific emphasis of the 2nd Party Auditing (Customer/Supplier Audits) and 3rd Party Auditing (Certification Bodies). During the delivery, the learner will complete a Consultant facilitated complete systematic audit of a QMS (Medical Devices.)

Learning Topics:

• Introduction to Auditing

• Introduction to QMS Auditing

• Compliance Auditing & Methodology

• Auditing Planning

• Opening Meeting

• Onsite Activities

• Auditing Report

• Completing the Audit

• Final Written QMS MD Examination

We are currently taking expressions of interest for this course.

Course Information
Venue Trainer Spaces Length
TBC Kelmac Group Available 5 days
Documentation
Title File
Course Content Download
Course Timetable
Date Times
Aug 20, 2018 8:00am to 5:30pm

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