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Training Matrix Template - ISO 13485

Training Matrix Template - ISO 13485

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ISO 13485:2016 Training Matrix Template (QMS.6.2.0.2 – QR)

Enhance your Quality Management System with our ISO 13485:2016 compliant Training Matrix Template, expertly crafted by the professionals at Patient Guard. Our Medical Device Quality Assurance and Regulatory Affairs document templates are developed by experienced experts, ensuring they meet the specific requirements of each clause and section of the relevant standards or regulations.

Why Choose Our Template?

  • Expertly Designed: Created by seasoned Quality Assurance and Regulatory Affairs specialists, our templates ensure full compliance with ISO 13485:2016 standards. Easy
  • Customization: Fully editable in Microsoft Word, our templates allow you complete control to modify and tailor them to your specific business needs and branding.
  • Compliance Assurance: Utilizing our template helps you maintain an effective training matrix, demonstrating robust quality management as required by ISO 13485:2016.

How Does the Training Matrix Help Us Achieve Compliance with ISO 13485?

ISO 13485 requires that organizations: Determine the necessary competence for personnel performing work affecting product quality.

Maintain appropriate records of education, training, skills, and experience. The Training Matrix is used to identify personnel to be trained on specific procedures or processes as described in QMS.6.2.0 – QP – Training & Qualifications Procedure. Along with QMS.6.2.0.3 – QR – Training Record and QMS.6.2.0.1 – QR – Employee Induction Template, this document provides evidence to demonstrate compliance with the requirements of the standard.

You will also be able to ensure and provide evidence that your employees have achieved the required competence to fulfill their roles.

How Else Can the Template Be Used?

To identify mandatory requirements for induction and company-wide training modules/workshops/presentations. To highlight training requirements for internal standard operating procedures and work instructions. To plan for any external training courses.

Why Patient Guard?

Stay ahead with Patient Guard’s consultancy services, offering a cost-effective solution for all your Quality Management System needs. For more templates and services in Medical Device Quality Assurance and Regulatory Affairs, or to provide feedback, contact us at qmsregs@patientguard.com.

Visit our blog for updates on regulatory and quality assurance news, and take the next step in enhancing your Quality Management System with Patient Guard.

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