Course information

ISO 13485 Lead Auditor Training Course Outline

Module 1: Introduction to ISO 13485:2016

  • Introduction
  • What is ISO 13485:2016?
  • Benefits of Implementing ISO 13485
  • Applications of ISO 13485
  • First Steps to ISO 13485:2016 Compliance
  • What is a Medical Device?
  • Purpose of a Quality Management System
  • Importance of ISO 13485
  • Basic Principles of ISO 13485
  • Exercise

Module 2: ISO 13485 Clauses 1 and 2

  • Clause 1 – Scope
  • Clause 5 - Management Responsibilities
  • Clause 6 - Resource Management
  • Clause 2 - Normative References

Module 3: ISO 13485 Clauses 3 and 4

  • Clause 3 - Terms and Definitions
  • Clause 4 - Quality Management System
  • Clause 4.1 General Requirements
  • Clause 4.2 Document Requirements
  • Exercise

Module 4: Requirements and Quality Systems

  • Requirements and Quality Systems
  • Clause 5 - Management Responsibilities
  • Clause 6 - Resource Management
  • Clause 7 - Product Realization
  • Clause 8 - Measurement, Analysis, and Improvement
  • Exercise

Module 5: Overview of ISO 13485:2016 Requirements

  • Requirements of ISO 13485:2016
  • General Requirements
  • Documentation Requirements
  • Management Responsibility
  • Resources
  • Product Realization
  • Infrastructure
  • Risk Management

Module 6: Implementation Phases of the ISO 13485 Frameworks

  • Stages to Implementation
  • Gap Analysis
  • Process Mapping

Module 7: Conducting an ISO 13485 Certification Audit

  • Certification Audits
  • Exercise

Module 8: Relationship Between ISO 13485 and ISO 9001

  • Scope
  • Focus
  • Continual Improvement
  • Terminology
  • Differences Between the Standards
  • Similarities Between the Standards

Module 9: Internal Auditing

  • Internal Auditing
  • Internal Audit Objectives
  • Auditing Skills
  • Steps in Internal Auditing
  • Planning, Preparation, and Management of Audits
  • Internal Audit – PDCA Cycle
  • Types of Audits
  • Audit Techniques
  • Exercise

Module 10: Internal Audit Plan

  • Audit Plan
  • Criteria

Module 11: Audit Process

  • Audit Process
  • Conducting Process Audits
  • Scope
  • Criteria
  • Reporting Audit Findings

Module 12: Internal Audit Evidence and Findings

  • Internal Audit Evidence and Findings
  • Classification
  • Closing Report
  • Nonconformities
  • Documented Procedure
  • Exercise

Module 13: Roles and Responsibilities

  • Internal Auditor Responsibilities
  • Closing Meetings

Module 14: Resource Management and Product Realization

  • Provision of Resources
  • Infrastructure
  • Planning and Development of Products

Module 15: ISO 13485 and Quality Management Systems

  • ISO 13485
  • Quality Management Systems (QMS)
  • Exercise

Module 16: Principles of Quality Management System

  • Principles of QMS
  • Exercise

Module 17: Fundamentals of Quality Management Systems

  • Fundamentals of Quality Management Systems

Module 18: Measurement, Analysis, and Improvement

  • Measurement, Analysis, and Improvement
  • General Requirements
  • Monitoring and Measurement
  • Control of Nonconforming Product
  • Performance of QMS
  • Analysis of Data
  • Improvement
  • Corrective Action
  • Preventive Action
  • Identification of Improvement Opportunities

Module 19: Risk Management

  • Risk Management
  • Risk Management Principle
  • Risk Management Process
  • Risk Lifecycle
  • Risk Management Tools
  • Risk Management Culture
  • Assessments and Control of Risk Management
  • Exercise

Module 20: Key Terms and Definitions of Lead Auditor

  • Key Terms Definitions

Module 21: Lead Auditor Responsibilities

  • Lead Auditor Responsibilities
  • Auditing Organization
  • Auditees

Module 22: Team Leader Skills

  • Team Leader Skills
  • Exercise

Module 23: Structure and Intent of ISO 13485

  • Structure and Intent
  • Clause 5 – Management Responsibility
  • Clause 6 – Resource Management
  • Clause 7 – Product Realization
  • Clause 8 – Measurement, Analysis, and Improvement

Module 24: Medical Devices, Quality, and Auditing Terminology

  • Medical Devices
  • Quality Management System
  • Auditing Terminology
  • Exercise

Module 25: Processes, Procedures, and Records

  • Processes
  • Procedure
  • Records

Module 26: Checklist Development

  • Purpose
  • Completed Checklist Provides
  • Process Based Audits
  • Checklist
  • Process Checklist

Module 27: Planning, Preparation, and Management of Audits

  • Planning
  • Preparation
  • Management of Audits
  • Exercise

Module 28: Interviewing Skills

  • Key Interviewing Skills
  • Star Technique

Module 29: Corrective Action and Verification

  • Overview
  • Corrective Action
  • Documented Procedure
  • Process

Module 30: Preventative Action

  • Overview
  • Preventive Action: Process
  • Exercise and Questions

Show moredowndown

Who should attend this ISO 13485 Lead Auditor Course?

The ISO 13485 Lead Auditor Course in Baton Rouge provides the knowledge and skills required to conduct audits of medical device Quality Management Systems against the requirements of ISO 13485. This course can be beneficial for professionals, including:

  • Lead Auditors
  • Quality Control Managers
  • Regulatory Affairs Managers
  • Compliance Officers
  • Manufacturing Managers
  • Quality Assurance Professionals
  • Internal Auditors

Prerequisites of the ISO 13485 Lead Auditor Course

There are no formal prerequisites for this ISO 13485 Lead Auditor Course. However, some knowledge of quality management systems, auditing techniques, and regulatory requirements, along with practical experience in medical device manufacturing, would greatly benefit the delegates.

ISO 13485 Lead Auditor Training Course Overview

ISO 13485 sets the standards for a Quality Management System (QMS) in scenarios where organizations need to consistently demonstrate their ability to provide medical devices and related services that meet customer and regulatory requirements. This training in Baton Rouge equips learners with the skills required for implementing a quality management system for medical devices and conducting audits to ensure organizational performance.

Acquiring knowledge from this ISO 13485 Training benefits organizations by streamlining processes and reducing operational challenges. Individuals in Baton Rouge pursuing this training can enhance their expertise and capabilities, opening new career opportunities and potential income growth. Professionals in roles that are responsible for quality management systems, should aspire to master ISO 13485 Lead Auditor training.

The Knowledge Academy's 5-day ISO 13485 Lead Auditor Training Course in Baton Rouge offers a comprehensive understanding of quality management and the art of auditing systems. Delegates will delve into the implementation phases of ISO frameworks and gain expertise in gap analysis to support various clauses. They will also explore risk management, learning how to map identified risks and monitor continuous improvement

Course Objectives:

  • To improve the quality of medical devices manufactured by a company
  • To promote harmonization of regulatory requirements for manufacturers
  • To provide access and evidence in accordance with regulatory requirements
  • To engage management actively and undertake management system activities
  • To protect the confidentiality of all documents and information obtained in the audit
  • To obtain quality objectives from the manufacturer and pass them to the organization

After completing this training in Baton Rouge, delegates will be able to implement this ISO standard by specifying company requirements and the scope of medical devices. They will also be able to take on responsibilities associated with auditing authority for the management and performance of all audit activities.

Show moredowndown

What’s included in this ISO 13485 Lead Auditor Course?

  • ISO 13485 Lead Auditor Examination
  • World-Class Training Sessions from Experienced Instructors
  • ISO 13485 Lead Auditor Certificate
  • Digital Delegate Pack

ISO 13485 Lead Auditor Exam Information

To achieve the ISO 13485 Lead Auditor, candidates will need to sit for an examination. The exam format is as follows: 

  • Question Type: Multiple Choice 
  • Total Questions: 30 
  • Total Marks: 30 Marks 
  • Pass Mark: 50%, or 15/30 Marks 
  • Duration: 40 Minutes  
  • Open Book/ Closed Book: Closed Book

Why choose us

Our Baton Rouge venue

Includes..

Free Wi-Fi

To make sure you’re always connected we offer completely free and easy to access wi-fi.

Air conditioned

To keep you comfortable during your course we offer a fully air conditioned environment.

Full IT support

IT support is on hand to sort out any unforseen issues that may arise.

Video equipment

This location has full video conferencing equipment.

Baton Rouge is the capital of the state of Louisiana, it has an estimated population of 230,000 people. The name of the city means “Red Stick” in French. Education in the USA is provided by both public and private schools, and is mandatory until the age of 16.  Pupils conducting their schooling within the USA start off at preschool, followed by elementary school, then middle school, before finishing at high school.  At age 18, US citizens are able to engage in higher education.  Higher education in the USA normally comes in the form of a college, undergraduate school, or a community college – that latter of which doesn’t normally cost anything to attend.  Candidates participating in a course at a college will gain credits towards a bachelor’s degree, whilst candidates participating a course at a community college will be earning credits in order to achieve an associate’s degree. The East Baton Rouge Parish Public Schools board oversees the running of the public primary and secondary schools in the city. There are a number of charter schools in the area, one of these is the Mentorship Academy. This school uses their relationship and proximity to local businesses to establish opportunities with them. Baton Rouge is also home to 9 U.S Blue Ribbon School and renowned Magnet Program for gifted children in specific areas. Louisiana State University is a public university with an enrollment of 32,000 students and 1,300 faculty members. It was founded in 1853 as a military academy. It is now officially known as Louisiana State University and Agricultural and Mechanical College. The college has schools in agriculture, art and design, engi9neering and science. At The Knowledge Academy we offer over 50,000 classroom based training courses in the United States, including popular locations such as Baton Rouge.

Show moredown

Address

301 North Main Street, 

Louisiana 70825, 

Baton Rouge, 

United States

T: +1 7204454674

Ways to take this course

Experience live, interactive learning from home with The Knowledge Academy's Online Instructor-led ISO 13485 Training | ISO 13485 Lead Auditor Training in Baton Rouge. Engage directly with expert instructors, mirroring the classroom schedule for a comprehensive learning journey. Enjoy the convenience of virtual learning without compromising on the quality of interaction.

Unlock your potential with The Knowledge Academy's ISO 13485 Training | ISO 13485 Lead Auditor Training in Baton Rouge, accessible anytime, anywhere on any device. Enjoy 90 days of online course access, extendable upon request, and benefit from the support of our expert trainers. Elevate your skills at your own pace with our Online Self-paced sessions.

Streamline large-scale training requirements with The Knowledge Academy's In-house/Onsite at your business premises. Experience expert-led classroom learning from the comfort of your workplace and engage professional development.

tailored_learning_experience

Tailored learning experience

Leverage benefits offered from a certification that fits your unique business or project needs

budget

Maximise your training budget

Cut unnecessary costs and focus your entire budget on what really matters, the training.

team_building

Team building opportunity

Our offers a unique chance for your team to bond and engage in discussions, enriching the learning experience beyond traditional classroom settings

monitor_progress

Monitor employees progress

The course know-how will help you track and evaluate your employees' progression and performance with relative ease

What our customers are saying

ISO 13485 Training | ISO 13485 Lead Auditor Training in Baton Rouge FAQs

An ISO 13485 Lead Auditor is a professional trained to audit and ensure compliance with ISO 13485, the international standard for medical instrument quality control systems. Completing this course equips you with the expertise to lead and manage audits effectively.
Implementing ISO 13485 in a company is essential to establish a comprehensive quality management system specifically designed for medical devices. This standard ensures adherence to regulatory requirements, enhances product safety, and promotes customer confidence, facilitating global market access for the company's medical devices.
Taking the ISO 13485 Lead Auditor Training enhances your ability to perform effective medical device quality management systems audits, ensuring compliance with global standards. It also improves your career prospects in the medical device industry.
The Lead Auditor is responsible for preparing audit reports, conducting interviews with company employees, reviewing company policies, and performing tests of controls.
The ISO 13485 Lead Auditor Training Course is ideal for quality professionals, regulatory personnel, and anyone involved in medical device auditing, manufacturing, or quality management systems who seek to enhance their expertise in auditing against the ISO 13485 standard.
Yes, to achieve this certification, candidates must successfully pass an examination. This exam assesses the individual's knowledge and understanding of the ISO 13485 standard and their ability to apply it in real-world audit scenarios.
In the ISO 13485 Lead Auditor Training, you’ll gain expertise in auditing medical device quality management systems, understanding ISO 13485 requirements, and leading audits effectively to ensure compliance with international standards, enhancing your auditing skills in the medical sector.
The ISO 13485 Lead Auditor Certification aims to equip professionals with the skills to audit and assess medical device quality management systems, ensuring they meet regulatory requirements and standards, ultimately enhancing product safety and effectiveness in the healthcare sector.
The ISO 13485 Lead Auditor Certification Course is moderately challenging. It requires a solid understanding of quality management systems and medical device regulations. It demands focus and dedication but is manageable for professionals with relevant industry experience.
There are no formal prerequisites for this ISO 13485 Lead Auditor Course. However, some knowledge of Quality Management Systems, auditing techniques, regulatory requirements, and practical experience in medical device manufacturing would significantly benefit the delegates.
Holding an ISO 13485 Lead Auditor Certification signifies expertise in auditing medical device quality management systems, ensuring compliance with regulatory standards. It's essential for professionals aiming to enhance their careers in the medical device industry.
In this training course, delegates will have intensive training with our experienced instructors, a digital delegate pack consisting of important notes related to this course, and a certificate after course completion, ensuring you gain practical experience and in-depth knowledge of ISO 13485 Lead Auditor.
This course takes 5 days to complete, during which delegates participate in intensive learning sessions that cover various course topics.
Yes, The Knowledge Academy offers 24/7 support via phone & email before attending, during, and after the course. Our customer support team is available to assist and promptly resolve any issues you may encounter.
The Knowledge Academy provides flexible self-paced training for this course. Self-paced training is beneficial for individuals who have an independent learning style and wish to study at their own pace and convenience.
Completing the ISO 13485 Lead Auditor Course can lead to roles such as Quality Manager, Compliance Officer, or Lead Auditor in the medical device industry. In these roles, you'll ensure regulatory compliance and effective quality management systems.
The ISO 13485 Lead Auditor Certification benefits individuals in quality management, regulatory affairs, and auditing roles, especially within the medical device industry. It equips them to ensure compliance and maintain high standards in quality management systems.
Yes, we provide corporate training for this course, tailored to fit your organisation’s requirements.
If you are unable to access your training course, contact the support team at The Knowledge Academy via their customer service email or phone number provided on their website for prompt assistance and resolution of your issue.
Taking the ISO 13485 Lead Auditor Course enhances your expertise in auditing medical device quality management systems, ensuring compliance with industry standards. It’s a valuable credential that boosts your career prospects in the medical device industry.
The ISO 13485 Lead Auditor Training Course requires delegates to understand the principles of ISO standards and quality management. This qualification is ideal for professionals involved in medical device manufacturing or regulatory affairs who want to enhance their auditing skills.
After completing the ISO 13485 Lead Auditor Training Course, you can pursue roles in quality management, lead audits in medical device industries, or enhance your current position by ensuring compliance with global standards in medical device manufacturing.
A background in other ISO 13485 courses is unnecessary to take ISO 13485 Lead Auditor Training, but it can be beneficial. The training covers essential auditing skills and ISO 13485 requirements, thoroughly preparing you.
The training fees for ISO 13485 Lead Auditorin Baton Rouge starts from $3195
The Knowledge Academy is the Leading global training provider for ISO 13485 Lead Auditor.
Show more down

Why choose us

icon

Best price in the industry

You won't find better value in the marketplace. If you do find a lower price, we will beat it.

icon

Many delivery methods

Flexible delivery methods are available depending on your learning style.

icon

High quality resources

Resources are included for a comprehensive learning experience.

barclays Logo
deloitte Logo
Thames Water Logo

"Really good course and well organised. Trainer was great with a sense of humour - his experience allowed a free flowing course, structured to help you gain as much information & relevant experience whilst helping prepare you for the exam"

Joshua Davies, Thames Water

santander logo
bmw Logo
Google Logo

Looking for more information on ISO 13485 Training?

backBack to course information

Get a custom course package

We may not have any package deals available including this course. If you enquire or give us a call on +1 7204454674 and speak to our training experts, we should be able to help you with your requirements.

cross

BIGGEST
BLACK FRIDAY SALE!

red-starWHO WILL BE FUNDING THE COURSE?

close

close

Thank you for your enquiry!

One of our training experts will be in touch shortly to go over your training requirements.

close

close

Press esc to close

close close

Back to course information

Thank you for your enquiry!

One of our training experts will be in touch shortly to go overy your training requirements.

close close

Thank you for your enquiry!

One of our training experts will be in touch shortly to go over your training requirements.