Globally Accredited Certified Internal Quality Auditor ISO13485:2016 Online course
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Certified Internal Auditor ISO13485:2016 (English)

Globally recognised and accredited Online Training and Certification course on Certified Internal Auditor - ISO13485:2016 (Medical Devices)

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Language: English

Instructors: Dr. Aryan Viswakarma

Validity Period: 365 days

$200 65.5% OFF

$69

PREVIEW

Why this course?

Description

Course: Certified Internal Auditor for ISO 13485

Course Duration: 18 hrs

Applicable Standard: ISO 13485: 2016

Course Objectives

To provide students with the knowledge and skills required to perform an internal audit of part of a quality management system based on ISO 13485: 2016 and report on the effective implementation and maintenance of the management system in accordance with the standard.

Prerequisites

It is recommended that all students have the following prior knowledge:

  1. Basic knowledge of the concepts of quality management and the relationship between quality management and customer satisfaction
  2. Understand quality management terms and definitions
  3. At least 1 year of industry experience

Who Should Attend?

This course is ideal for those who are responsible for internal management system audits including department managers, supervisors, quality representatives, engineers, and administrative staff who have a focus on business improvement, performance, and profitability.

Join Our Weekly Live Doubt-Clearing Sessions

We are committed to your learning success! To ensure clarity and help you achieve your goals, we conduct live doubt-clearing sessions every week.

Why Attend?

  • Get personalized answers to your questions.
  • Clarify doubts on complex concepts or assignments.
  • Interact directly with our expert instructors.
  • Strengthen your understanding and confidence.

Certification Exam Guidelines

Examination Format:

  • The certification exam comprises multiple-choice and descriptive questions designed to assess the comprehension of the Body of Knowledge.
  • The exam will be conducted online and is available only in English.

Course Validity & Exam Timeline:

  • Learners must take the final exam within 12 months of purchasing the course.
  • Course access will remain available throughout the designated access period as applicable.

Note: Attempting the exam after the one-year period will require an additional fee.

Certification:

  • E-certificates will be issued upon successful completion of the exam.
  • Certificates will be delivered within 7 working days after passing the exam.

Sample Certificate:

Policy on Cancellation and Refunds

  • The course to which you have subscribed cannot be replaced with another course.
  • It is not possible to cancel a course once it has been purchased.
  • There are no refunds for fees.
  • Courses are not transferrable.
  • Course Extension is possible. (How to seek a course extension, details are listed below)

For Technical Support-

Contact us at +91-8094078781  or drop a mail at [email protected]

*Prices may change at any time without prior notice.

REQUEST FOR COURSE VALIDITY EXTENSION

  • STEP 1 - Select the validity period for a course extension
  • STEP 2 - Pay and Share screenshot on Mail: [email protected]

    

You can also pay by scanning a QR code. Kindly share a screenshot by mail at [email protected] with full details after payment (Name, Email id, Contact No. and Course Name)

Benefits of Doing Courses from Quality HUB India™

  • Expert instruction: Quality HUB India has a team of experienced trainers and consultants who have extensive knowledge and practical experience in their respective fields.
  • Relevant and up-to-date content: Quality HUB India courses are designed to be practical and relevant, and they are updated regularly to reflect the latest best practices and industry standards.
  • Industry recognition: Quality HUB India courses are recognized by various organizations and institutions in the industry, which can enhance your credibility and help you to stand out in the job market.
  • Online Weekly Live Doubt Clearing Session: Interact with the faculty online every week and clarify your doubts arising during the learning for one full year from the date of purchasing the course.
  • Networking opportunities: Quality HUB India courses provide opportunities for attendees to network with professionals from different industries and backgrounds, which can help you build valuable relationships and expand your knowledge.
  • Flexible learning options: Quality HUB India offers both online and classroom-based courses, which provides flexibility for busy professionals and allows you to choose the learning option that best fits your schedule and preferences.
  • Affordable pricing: Quality HUB India courses are priced affordably, making them accessible to individuals and organizations of all sizes and budgets.

Awards & Recognitions

  • “Indian Achiever’s Award 2021-22” by Indian Achiever’s Forum
  • ‘THE 2022 Global Education Award’ by Xel Research & Journey Magazine
  • “Top 10 Manufacturing Consultant 2022” by Industry Outlook Magazine
  • “THE BEST Learning Platform of 2022” by Business Connect Magazine

Accreditations & Certifications

  • The Council for Six Sigma Certification (CSSC) – USA
  • International Quality Federation (IQF) – USA
  • International Accreditation Organisation (IAO) – USA
  • ISO 9001:2015 – Quality Management System
  • ISO 14001:2015 – Environment Management System
  • ISO 29990:2010 – Learning Services for Non-Formal Education & Training

Course Curriculum

    Introduction to ISO13485

  • Introduction to Medical Device Standard
  • ISO13485 – Benefits, Exclusion, and Non-Applicability
  • Introduction to Standard
  • Clarification of the Concept
  • Process and Process Approach
  • ISO13485 Compatibility with other management systems
  • ISO13485 Standard and Clauses

  • Introduction to ISO13485 Standard and Clauses
  • Scope (Clause 1) and Normative Reference (Clause 2)
  • Clause 3.0 Terms and Definition
  • Clause 4.0 Quality Management System
  • Clause 5.0 Management Responsibility
  • Clause 6.0 Resource Management
  • Clause 7.0 Product Realization
  • Clause 8.0 Measurement, Analysis, and Improvement
  • ISO19011:2018 – Guideline for Conducting Audit

  • Guideline for Conducting Audit
  • Clause 3 (Terms and Definitions)
  • Clause 4 (Principles of Auditing)
  • Clause 5 (Managing an Audit Program)
  • Internal Audit Schedule
  • Clause 6 Performing an Audit
  • Clause 6 Audit Check List
  • Clause 6 Performing an Audit
  • Clause 6 Interviewing Technique
  • Clause 6 Conducting the audit
  • Clause 6.4.2 – Third-Party Opening Meeting
  • Clause 6.4.7 – Collecting Information
  • Clause 6.4.8 (Generating Audit Findings)
  • Clause 6 (Audit Reporting
  • Clause 6 (NC Reports)
  • Clause 6 Closing of Audit
  • Clause 7 (Control of Audit)
  • Clause 7(Auditor Competency)
  • Non Conformity(NC) Report Writing
    • Content of NC Report
    • Non-Conformity Report Format
    • NC Report ISO13485 NC case Study
    • · Most Common NCRs observed during ISO13485 Audit

    Other Support Modules

  • Levels of Documents
  • Types of Processes: COP, MOP, and SOP
  • Quality Objective Tracker System
  • Important Audit Terms and Definitions
  • What is an Audit? Types of System Audits
  • Difference between `System’ and `Process’
  • Management Review Meeting (MRM)
  • Roles and Responsibilities of an MR
  • Practice Test Paper

    Supporting PDF, Formats, Standards, etc. provided for study and reference purpose

    Additional Resources

  • pdf file- 06 no.
  • Format- 01 no.
  • ebook- 02 no.

How to Use

After successful purchase, this item would be added to your courses.You can access your courses in the following ways :

  • From the computer, you can access your courses after successful login
  • For other devices, you can access your library using this web app through browser of your device.

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