Why should you attend?
ISO 13485 Lead Implementer training enables you to develop the necessary expertise to support an organization in establishing, implementing, managing and maintaining a Medical Devices Quality Management System (MDQMS) based on ISO 13485. During this training course, you will also gain a thorough understanding of the best practices of Medical Devices Quality Management Systems and be able to improve an organization`s overall performance by consistently providing safe and qualitative medical devices.
After mastering all the necessary concepts of Medical Devices Quality Management Systems, you can sit for the exam and apply for a “PECB Certified ISO 13485 Lead Implementer” credential. By holding a PECB Lead Implementer Certificate, you will be able to demonstrate that you have the practical knowledge and professional capabilities to implement ISO 13485 in an organization.
Who should attend?
Learning objectives
Educational approach
Prerequisites
A fundamental understanding of ISO 13485 and comprehensive knowledge of implementation principles.
Day 1: Introduction to ISO 13485 and initiation of a MDQMS
Day 2: Plan the implementation of a MDQMS
Day 3: Implementation of a MDQMS
Day 4: MDQMS monitoring, measurement, continuous improvement and preparation for a certification audit
Day 5: Certification Exam
After successfully completing the exam, you can apply for the credentials shown on the table below. You will receive a certificate once you comply with all the requirements related to the selected credential. For more information about ISO 13485 certifications and the PECB certification process, please refer to the Certification Rules and Policies.
The requirements for PECB Implementer Certifications are:
Credential | Exam | Professional experience | MDQMMS project experience | Other requirements |
PECB Certified ISO 13485 Provisional Implementer | PECB Certified ISO 13483 Lead Implementer Exam or equivalent | None | None | Signing the PECB Code of Ethics |
PECB Certified ISO 13485 Implementer | PECB Certified ISO 13483 Lead Implementer Exam or equivalent | Two Years: One year of work experience in Medical Devices Quality Management | Project activities: a total of 200 hours | Signing the PECB Code of Ethics |
PECB Certified ISO 13485 Lead Implementer | PECB Certified ISO 13483 Lead Implementer Exam or equivalent | Five Years: Two years of work experience in Medical Devices Quality Management | Project activities: a total of 300 hours | Signing the PECB Code of Ethics |
PECB Certified ISO 13485 Senior Lead Implementer | PECB Certified ISO 13483 Lead Implementer Exam or equivalent | Ten Years: Seven years of work experience in Medical Devices Quality Management | Project activities: a total of 1,000 hours | Signing the PECB Code of Ethics |
Note: PECB Certified Individuals who do possess the Lead Implementer and Lead Auditor Credentials are qualified for the respective PECB Master Credential, given they have taken 4 additional Foundation Exams which are related to this scheme. For more detailed information about the Foundation Exams and the overall Master Requirements, please go to the following link: https://pecb.com/en/master-credentials.
To be considered valid, these implementation activities should follow best implementation practices and include the following activities:
Drafting a MDQMS plan
Initiating a MDQMS implementation
Implementing a MDQMS
Monitoring and managing a MDQMS implementation
After successfully completing the exam, you can apply for the credential shown on the table below.
The certificate requirements for the ISO 13485 Foundation are:
Designation | Exam | Professional experience | MS audit/assessment experience | MDQMMS project experience | Other requirements |
PECB Certificate Holder in ISO 13485 Foundation | Pass the PECB ISO 13485 Foundation Exam | None | None | None | Signing the PECB Code of Ethics |
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