Certify your expertise with ISO 13485 Internal Auditor Certificate
Given the sensitivity of the medical industry, adherence to regulatory standards is vital for ensuring the safety and efficacy of medical devices. ISO 13485 is the internationally recognized quality management system standard for the medical device industry. It demonstrates to customers that the company maintains high standards for quality. Additionally, it assures them that the business has established procedures to ensure compliance. Professionals with ISO 13485 Internal Auditor Certificate play a crucial role in ensuring the organization complies with all standard requirements. They evaluate and enhance their adherence to regulatory requirements, lowering the possibility of non-compliance issues and regulatory penalties. This expertise enables them to secure lucrative jobs and increase their professional profile. Additionally, being certified in ISO 13485 is highly valuable and acknowledged globally.
Discover the strategic advantages of ISO 13485 for your business
In the current business environment, clients firmly believe that companies with an effective MDQMS are more trustworthy than those that are not. This is one of the main reasons medical device manufacturers must follow the ISO 13485 standard. This standard assists them in developing a QMS that improves and maintains the effectiveness of their operations. It guarantees medical devices are systematically designed, developed, produced, installed, delivered, and disposed of while ensuring their safety and intended purpose. Employing an ISO 13485 Internal Auditor becomes a necessity for organizations to maintain quality, compliance, and continual improvement in their operations. This also aids them in reaching global customers and taking advantage of new business prospects.
Elevate your audit skills with ISO 13485 Internal Auditor Training In South Korea?
ISO 13485 Medical Devices Quality Management System Training in South Korea teaches participants to plan and schedule an internal audit program for medical device quality management systems. It also imparts information on auditing methods, audit concepts, organizing, conducting, and reporting audits. It also discusses the main duties of an auditor as well as the structure and scope of the standard. Participants in ISO 13485 Training acquire an awareness of ISO 13485 requirements and how they relate to organizations seeking to comply with regulations. This knowledge enables them to assess the current state of the Quality Management System and processes effectively. Upon completion, candidates must pass an exam to demonstrate proficiency in QMS internal auditing. Successful candidates receive a certificate, validating their expertise in ISO 13485.
Corporate Group Training
- Customized Training
- Live Instructor-led
- Onsite / Online
- Flexible Dates
ISO 13485 Internal Auditor Exam Format | |
Exam Name | ISO 13485 Internal Auditor Certification |
Exam Format | Multiple choice |
Total Questions | 30 MCQs |
Passing Score | 70% |
Exam Duration | 60 minutes |
Key features of ISO 13485 Internal Auditor Certification Training in South Korea
ISO 13485 Course provides a thorough understanding of quality management system requirements under ISO 13485. Our training program is delivered by seasoned experts with extensive knowledge in ISO 13485 internal audits. They ensure participants understand how ISO 13485 applies to their organization's regulatory requirements. Additionally, training course includes hands-on exercises and case studies. This enables trainees to use auditing principles and methods in practical settings. We deliver ISO 13485 Certification Training in South Korea through live online instructor-led sessions and in-classroom methods. This gives participants the option to select the format that best suits their learning style and schedule. Our course ensures trainees gain expertise and confidence to excel in auditing medical device quality management systems.
- 2 Day Interactive Instructor –led Online Classroom or Group Training in South Korea
- Course study materials designed by subject matter experts
- Mock Tests to prepare in a best way
- Highly qualified, expert & accredited trainers with vast experience
- Enrich with Industry best practices and case studies and present trends
- ISO 13485 Internal Auditor Training Course adhered with International Standards
- End-to-end support via phone, mail, and chat
- Convenient Weekday/Weekend ISO 13485 Internal Auditor Training Course schedule in South Korea
ISO 13485 Internal Auditor Certification Benefits
Higher Salary
With this renowned credential, aspirants earn higher salary packages when compared to non-certified professionals in the field
Individual accomplishments
Aspirants can look for higher career prospects at an early stage in their life with the most esteemed certification
Gain credibility
Owning the certification makes it easier to earn the trust and respect of professionals working in the same field
Rigorous study plan
The course content is prescribed as per the exam requirements, covering the necessary topics to ace the exam in the first attempt
Diverse job roles
Attaining the certification enhances the spirit of individuals to pursue diverse job roles in the organization
Sophisticated skillset
With this certification, individuals acquire refined skills and techniques required to play their part in an organization
ISO 13485 Internal Auditor Course Curriculum
-
Module 1: Introduction to ISO 13485:2016
Topics
- · 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
Topics
- · Clause 1 – Scope
- · Clause 5 - Management Responsibilities
- · Clause 6 - Resource Management
- · Clause 2 - Normative References
-
Module 3: ISO 13485 Clauses 3 and 4
Topics
- · 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
Topics
- · Requirements and Quality Systems
- · Clause 5 - Management Responsibilities
- · Clause 6 - Resource Management
- · Clause 7 - Product Realisation
- · Clause 8 - Measurement, Analysis, and Improvement
- · Exercise
-
Module 5: Overview of ISO 13485:2016 Requirements
Topics
- · Requirements of ISO 13485:2016
- · General Requirements
- · Documentation Requirements
- · Management Responsibility
- · Resources
- · Product Realisation
- · Infrastructure
- · Risk Management
-
Module 6: Implementation Phases of the ISO 13485 Frameworks
Topics
- · Stages to Implementation
- · Gap Analysis
- · Process Mapping
-
Module 7: Conducting an ISO 13485 Certification Audit
Topics
- · Certification Audits
- · Exercise
-
Module 8: Relationship Between ISO 13485 and ISO 9001
Topics
- · Scope
- · Focus
- · Continual Improvement
- · Terminology
- · Differences Between the Standards
- · Similarities Between the Standards
-
Module 9: Internal Auditing
Topics
- · Internal Auditing
- · Internal Audit Objectives
- · Auditing Skills
- · Steps in Internal Auditing
- · Planning, Preparation, and Management of Audits
- · Internal Audit – PDCA Cycle
- · Types of Audit
- · Audit Techniques
- · Exercise
-
Module 10: Internal Audit Plan
Topics
- · Audit Plan
- · Criteria
-
Module 11: Audit Process
Topics
- · Audit Process
- · Conducting Process Audits
- · Scope
- · Criteria
- · Reporting Audit Findings
-
Module 12: Internal Audit Evidence and Findings
Topics
- · Internal Audit Evidence and Findings
- · Classification
- · Closing Report
- · Nonconformities
- · Documented Procedure
- · Exercise
-
Module 13: Roles and Responsibilities
Topics
- · Introduction
- · Internal Auditor Responsibilities
- · Closing Meetings
-
Module 14: Resource Management and Product Realisation
Topics
- · Provision of Resources
- · Infrastructure
- · Planning and Development of Products
Frequently Asked Questions
What are the learning objectives of ISO 13485 Internal Auditor Training in South Korea?
Participants in training learn to perform internal audits for medical device Quality Management Systems. They also gain knowledge in auditing methods, audit concepts, scheduling, conducting, and reporting audits. Additionally, they learn the structure and scope of the standard.
Will ISO 13485 Training impart practical skills to candidates?
Yes, training gives candidates hands-on experience in conducting internal audits QMS as per ISO 13485 standard. This allows them to apply these skills in real-life scenarios.
What are the skills gained through ISO 13485 Course?
Individuals gain skills in performing internal audits, communication skills, leadership skills, problem-solving skills, risk management skills, and analytical skills.
What is the format of ISO 13485 Quality Management System Training in South Korea?
ISO 13485 Quality Management System Training in South Korea is offered in both live online instructor-led sessions and in-classroom methods.
Will ISO 13485 Internal Auditor Training Online broaden my skills?
Training offers in-depth knowledge of the ISO 13485 standard, its requirements, the audit process, and best practices for implementing and maintaining a QMS. These all broaden their skills for conducting audits within an organization.
Will I gain leadership skills through ISO 13485 Training?
Training equips individuals with leadership skills, allowing them to lead audit teams and collaborate with cross-functional teams effectively.
How do ISO 13485 Course support candidates in identifying risks?
Training program offers knowledge in identifying and assessing risks within the Quality Management System. This aids trainees in identifying and mitigating potential risks and ensuring the safety and effectiveness of medical devices.
What is the format of ISO 13485 Internal Auditor Exam?
ISO 13485 Internal Auditor Exam consists of thirty multiple-choice questions. Candidates have to complete it in 60 minutes.
How much does ISO 13485 Exam in South Korea cost?
Candidates do not have to incur ISO 13485 Exam fees. It is included in the ISO 13485 Internal Auditor Training fee.
What does ISO 13485 Quality Management System Exam evaluate?
The exam evaluates candidates' knowledge in ISO 13485 requirements. It also assesses their skills in auditing methods, audit concepts, scheduling, conducting, and reporting audits.
How can I prepare for ISO 13485 Internal Auditor Exam?
The expertise gained ISO 13485 requirements and audit procedures in training is sufficient for candidates to pass the exam.
What is the pass score for ISO 13485 Quality Management System in South Korea?
The pass score for ISO 13485 Quality Management System in South Korea is 70%.
When will I receive my ISO 13485 Internal Auditor Exam result?
Aspirants will receive their ISO 13485 Internal Auditor Exam result as soon as they complete their exam.
When can I take ISO 13485 Exam?
Individuals can take ISO 13485 Exam after completing ISO 13485 Internal Auditor Training offered by Unichrone.
What is the cost of ISO 13485 Internal Auditor Certification in South Korea?
There is no separate cost for ISO 13485 Internal Auditor Certification in South Korea offered by Unichrone, it is included in the training fee.
How to get ISO 13485 Certification?
The following are the steps involved in getting ISO 13485 Certification
- Understand the standard
- Gap analysis
- Internal audit
- Meeting regulatory requirements
- Corrective actions
- Management review
- Certification audit
- Obtain the ISO 13485 Certification.
Is ISO 13485 mandatory for medical devices?
ISO 13485 is a voluntary standard. However, it is required for medical device manufacturers in countries such as Canada, Japan, Europe, the UK, the USA, Australia, Singapore, and Malaysia.
What is the current version of ISO 13485?
The current version of ISO 13485 is ISO 13485:2016. This version emphasizes risk management and risk-based decision-making.
How to maintain ISO 13485 Internal Auditor Certification?
Professionals do not need to maintain ISO 13485 Internal Auditor Certification, as it is valid for a lifetime.
Will ISO 13485 Certificate guarantee employment?
ISO 13485 Certificate enhances an aspirant's skills and knowledge in auditing methods, audit concepts, scheduling, conducting, and reporting audits. This helps them to stand out from non-certified individuals and increase employment opportunities.
How much salary is offered to certified Internal Auditors?
The average salary offered to certified Internal Auditors is USD 70K. However, this may vary due to job role, experience, and location.
ISO 13485 Internal Auditor Examination Procedure
PREPARE
Go through the intense 2-day ISO 13485 Internal Auditor Training offered by Unichrone. Fulfil all the requirements before the examination.
APPLY
Apply for the ISO 13485 Internal Auditor Exam conducted by Unichrone. Choose the suitable date for the exam.
ACQUIRE
Get certified with ISO 13485 Internal Auditor after clearing the exam. You will receive an email confirming the status.
What our customers say
Register for a free session with our trainer
Select your city to view ISO 13485 Internal Auditor Certification Training Course Schedule in South Korea
Faculty and Mentors
Our certified and highly experienced trainers are handpicked from various industries to assist aspirants with practical insights into the field, thereby providing a comprehensive understanding of fundamentals and complex terminologies
1200+
Instructors
20+
Minimum Experience
100+
Session Expertise
- Scope
- Normative References
- Terms and Definitions
- General requirements
- Management responsibility
- Resource management
- Product realization
- Measurement, analysis and improvement.
Base
Understand the fundamentals
Accede
Recognize your talent
Acquiesce
Be awarded
Admit