CQI / IRCA Approved Online Lead Auditor Training Program on ISO 13485 : 2016 Medical Devices Quality Management System

CQI / IRCA Approved Online Lead Auditor Training Program on ISO 13485 : 2016 Medical Devices Quality Management System

Feature:

  • This is a CQI/IRCA approved course on MDQMS – ISO 13485:2016 Lead Auditor 
  • Course is in accordance with ISO 19011 and ISO/IEC 17021
  • Learn practical approach to plan, effectively conduct and report first party, second party and third party audits of MDQMS.
  • The course focuses on imparting knowledge and developing skills in conducting audits of MDQMS effectively and independently as a team leader
     

Course Objectives

  • To understand the overview of ISO 13485:2016 – Medical Devices - Quality Management System (MDQMS)
  • To enable delegates understand key concepts in Medical Devices - Quality Management System (MDQMS) auditing
  • To impart/enhance practical auditing skills to become certificated Lead Auditor
  • To enhance the technical and behavioural competency in conducting effective MDQMS audits as Lead Auditor
     

Date and Time

Date : 3rd to 7th March, 2025

Time : 9:00 AM to 6:00 PM

Who should attend ?
  • Individuals aspiring to become certificated auditors/ lead auditors to make career in MDQMS auditing 
  • Medical device quality professionals interested in conducting first party, second party, and/or third party audits
  • MDQMS management representatives
  • Individuals responsible for managing the audit programs in their organization
  • Departmental / functional MDQMS coordinators
  • Existing internal auditors of MDQMS
  • Quality directors, managers, and engineers
  • Medical Devices - Quality Management System (MDQMS) Consultants
     
Prerequisite/Prior knowledge

All the delegates / participants are expected to have basic knowledge of the principles and concepts of Medical Devices - Quality Management System (MDQMS) including awareness of the need for quality in medical devices, responsibilities, management commitments, terms, definitions and requirements of ISO 13485:2016

Certificate

Certificate of successful completion shall be issued to all the delegates/participants who attend entire duration of the course, in all the sessions and qualify in examination.

Duration

8 Hours including 1 hour break Each Day

Registration Fees

Rs. 32,000/- + GST

Registration and Payment

https://pay.tuv-india.com/index1.php?mtid=117187

Registration with confirmed payment will be closed 24 Hours before the scheduled time of Webinar.

Refund Policy

In case of refund due to not attending the training / training got cancelled, the amount will be processed within 15 working days. You are requested to provide your complete bank details & cancel cheque copy for processing the refund.

        

We look forward to receiving your enquiry