ISO 13485 Medical Devices Quality Management Systems
The ISO 13485 Lead Implementer Certification in Ecuador demonstrates that professionals are capable of implementing MDQMS. Certified professionals engage in designing, maintaining, and managing the Medical Device Quality Management System as per the ISO standard. Organizations certified with ISO 13485 recruit certified ISO professionals for applying the standard. Professionals owning ISO 13485 Lead Implementer Certification assist businesses in meeting the requirements whilst applying the latest practices. The ISO 13485 Standard was designed to maintain the quality levels of medical devices and related services. Owning the certification further helps businesses to take advantage of foreign markets and clientele. The ISO 13485 standard was last revised in 2016. As a result, professionals comply with the requirements stated in ISO 13485:2016 while implementing the standard.
ISO 13485 Lead Implementer Training in Ecuador
The ISO 13485 Lead Implementer Training in Ecuador is offered by Unichrone through qualified trainers. Candidates enrolling in ISO 13485 Lead Implementer Training sessions are trained to be industry-ready while looking for career options. The ISO 13485 Certification is recognized across various nations. This assists individuals to look for opportunities on a global scale. The ISO 13485 Lead Implementer Training outline reflects the latest changes in the standard. As a result, professionals pursuing the certification can apply the best practices of quality management for medical devices. The prerequisite for pursuing the lead implementer certification in Ecuador is to obtain ISO 13485 Foundation Certification.
Key Features of ISO 13485 Lead Implementer Certification Training
ISO 13485 Lead Implementer Certification Training is hosted for 3 days across various cities in Ecuador. Candidates can opt for live online or in-class training methods. During the training sessions, individuals gain a comprehensive understanding of the standard, its approach, procedures, and techniques for implementation. The interactive sessions assist participants in grasping complex concepts easily. On completion of the training session, individuals can take up the ISO 13485 Lead Implementer Exam and score the required passing percentage. Candidates who clear the exam obtain their ISO 13485 Lead Implementer exam from TUV-SUD.
- 4 Day Interactive Instructor –led Online Classroom or Group Training in Ecuador
- 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
- ISO 13485 Lead Implementer Course adhered with International Standards
- End-to-end support via phone, mail, and chat
- Convenient Weekday/Weekend ISO 13485 Lead Implementer Training Course schedule in Ecuador
Corporate Group Training
- Customized Training
- Live Instructor-led
- Onsite / Online
- Flexible Dates
|ISO 13485 Lead Implementer Exam Format|
|Exam Name||ISO 13485 Lead Implementer Certification|
|Exam Format||Multiple Choice|
|Total Questions||100 Questions|
|Passing Score||70% of Total Score|
|Exam Duration||120 Minutes|
ISO 13485 Lead Implementer Certification Benefits
With this renowned credential, aspirants earn higher salary packages when compared to non-certified professionals in the field
Aspirants can look for higher career prospects at an early stage in their life with the most esteemed certification
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
With this certification, individuals acquire refined skills and techniques required to play their part in an organization
ISO 13485 Lead Implementer Course Curriculum
1.Introduction to ISO 13485:2016
- · What is ISO 13485:2016?
- · Importance of ISO 13485 for an organisation
2.A Overview of ISO 13485:2016 Requirements
- · General requirements
- · Documentation requirements
- · Management responsibility
- · Resources
- · Product realisation
- · Infrastructure
- · Risk management
3.Implementation Phases of the ISO 13485 Frameworks
- · Stages to implementation
- · Gap analysis
- Process mapping
4.Conducting an ISO 13485 Certification Audit
- · Certification audits
5.The Relationship Between ISO 13485 and ISO 9001
- · Scope
- · Focus
- · Continual improvement
- · Terminology
- · Differences between the standards
- · Similarities between ISO 13485 and ISO 9001
- · Internal audit objectives
- · Auditing skills
- · Internal audit objectives
- · Internal audit objectives
- · Records and follow-ups
- · Using correct procedures in reference to the 9001:2015 standard
7.Internal Audit Plan
- · The audit plan
- · Criteria
8.The Audit Process
- · Conducting process audits
- · Internal audit scope and criteria
- · Reporting audit findings
9.Internal Audit Evidence and Findings
- · Classification
- · The closing report
- · Nonconformities
- · Documented procedure
10.Roles and Responsibilities
- · Internal Auditor responsibilities
- · Closing meeting
- · Management responsibilities
11.Resource Management and Product Realisation
- · Provision of resources
- · Infrastructure
- · Planning and development of products
12.ISO 13485 and Quality Management Systems
13.Principles of Quality Management System
- · Customer and regulatory focus
- · Leadership
- · Involvement
- · The process approach
- · Common tools
- · Decision making
- · Supplier management
- · System management
- · Continuous improvement
14.Fundamentals of Quality Management Systems
15.Requirements and Quality Systems
16.Measurement, Analysis, and Improvement
- · Monitoring and measurement
- · Control of non-conforming products
- · The performance of the QMS
- · Analysis of data
- · Improvement of quality
- · Corrective action
- · Preventive action
- · Identification of improvement opportunities
- · Risk management principles
- · The risk management process
- · Risk lifecycle
- · Risk management tools
- · Risk management culture
- · Assessments and control of risk management
Frequently Asked Questions
How is ISO 13485 Lead Implementer Training conducted in Ecuador?
The ISO 13485 Lead Implementer Training in Ecuador is offered in live online method and in-class method by Unichrone.
How will I benefit from ISO 13485 Lead Implementer Training in Ecuador?
The ISO 13485 Lead Implementer Training sessions are provided in flexible modes. Our trainers provide real-time insights on the ISO standard. This helps candidates to gain a deeper understanding of the standard and its approach. Furthermore, the training sessions are designed to prepare individuals to be industry-ready through practical exercises.
What are the prerequisites for attending ISO 13485 Lead Implementer Training in Ecuador?
Individuals need to obtain ISO 13485 Foundation Certification before attending the ISO 13485 Lead Implementer Training sessions.
When can I take up mock tests?
Candidates can take up the mock tests at the end of the ISO 13485 Lead implementer Training session.
When is the ISO 13485 Lead Implementer Exam scheduled in Ecuador?
The ISO 13485 Lead Implementer Exam is scheduled at the end of the training session.
Can I retake the exam if I fail to clear the exam in the first attempt?
Yes, candidates can retake the exam without incurring any cost for the second time. For the subsequent attempts after 2nd attempt, candidates have to pay the re-examination fees.
How can I pass the ISO 13485 Lead Implementer Exam in Ecuador?
Individuals need to score 70% or more to clear the exam and obtain the ISO certification.
What is ISO 13485 Lead Implementer Certification?
ISO 13485 Lead Implementer Certification enhances the skills of individuals. The certification is designed to help individuals in broadening their knowledge of the standard, its requirements, approach, procedures, tools, and techniques. In addition, the certification also helps individuals to interpret the relation of ISO 13485 with other regulatory frameworks.
Who can pursue the ISO 13485 Lead Implementer Certification in Ecuador?
Managers, expert advisors, MDQMS team members, and any individual who is involved in maintaining MDQMS can pursue the certification in Ecuador.
What is the process of earning ISO 13485 Lead Implementer Certification in Ecuador?
Individuals who meet the eligibility criterion can enroll for the ISO 13485 Lead Implementer Training in Ecuador. Upon completion of the training session, participants can take up the exam. Individuals who score the required minimum passing percentage can acquire the certification.
What is the role of ISO 13485 certified Lead Implementer?
A certified ISO 13485 Lead Implementer is responsible for:
- Developing and maintaining a medical device quality management system
- Analyzing the requirements of the ISO standard
- Interpreting the connection of ISO 13485 with other standards and frameworks
- Help organizations in implementing the standard its requirements.
ISO 13485 Lead Implementer Examination Procedure
Attend intense 4 day ISO 13485 Lead Implementer Training offered by Unichrone. Fulfil all the requirements specified by the TUV-SUD before the examination.
Apply for the ISO 13485 Lead Implementer Exam, conducted by Unichrone, whilst filling up all necessary details. Attend the exam scheduled at the end of the training session.
Score the minimum score to get certified after in the exam. You will receive an email confirming the status.
What our customers say
Very engaging course with real world context and wonderful examples. Helped to expand my knowledge as a direct result of it.
Super awesome faculty! The best part of the training was lots of real time case studies and interactive sessions. Learnt many new concepts.
Technical Director MCI Ltd
Interesting, Focused, Real life case studies. The material was a comprehensive presentation of Lean principles and Six Sigma.
Head Of Operations
Really interesting, a lot of knowledge about processes, in many areas and departments, helped to understand the subjects easily.
I opted for Instructor led Online Session. The training was very well executed. It was awesome and exceeded my expectations.
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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