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ISO 9001:2015 QMS Template – Quality Policy Template (QMS.5.2.1.2 – QR) Enhance your Quality Management System with our ISO 9001:2015 compliant Quality Policy Template. Created by the fully qualified and experienced professionals at Patient Guard, this template meets the specific requirements of each clause and section of the ISO 9001:2015 standard. Why Choose Our Quality…
ISO 9001:2015 QMS Template – Receiving Inspection Goods In and Out (QMS.8.6 – QP) Enhance your Quality Management System with our ISO 9001:2015 compliant Receiving Inspection Goods In and Out template. Created by the fully qualified and experienced professionals at Patient Guard, this template meets the specific requirements of each clause and section of the…
ISO 13485:2016 QMS Template – Reporting to Regulatory Authorities Vigilance Procedure (QMS.8.2.3 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Vigilance Procedure 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…
ISO 13485:2016 QMS Template – Requirements for Product Installation Activities Procedure (QMS.7.5.3 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Requirements for Product Installation Activities Procedure 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…
ISO 13485:2016 QMS Template – Requirements for Servicing Activities (QMS.7.5.4-QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Requirements for Servicing Activities Procedure 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…
ISO 13485:2016 QMS Template – Requirements for the Cleanliness of Product (QMS.7.5.2 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Requirements for the Cleanliness of Product 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…
ISO 9001:2015 QMS Template – Resource Management (QMS.7.1 – QP) Enhance your Quality Management System with our ISO 9001:2015 compliant Resource Management template. Created by the fully qualified and experienced professionals at Patient Guard, this template meets the specific requirements of each clause and section of the ISO 9001:2015 standard. Why Choose Our Resource Management…
ISO 13485:2016 QMS Template – Rework Procedure (QMS.8.3.4 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Rework Procedure 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…
Risk Evaluation and Risk-Benefit Analysis Template – ISO 14971 Our Risk Evaluation and Risk-Benefit allows you to achieve effective and compliant risk management with our Risk Evaluation and Risk-Benefit Analysis Template. This template is specifically designed to align with ISO 14971 standards, making it easier to navigate the complex process of risk evaluation and risk-benefit…
ISO 13485:2016 QMS Template – Risk Management Procedure (QMS.7.1.0 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Risk Management Procedure 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…
ISO 13485:2016 QMS Template – Software Acceptance Testing Plan and Record (QMS.4.1.6.2 – QT) Enhance your Quality Management System with our ISO 13485:2016 compliant Software Acceptance Testing Plan and Record 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…
ISO 13485:2016 QMS Template – Software Validation and Re-validation Procedure (QMS.4.1.6 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Software Validation and Re-validation Procedure 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…
ISO 13485:2016 QMS Template – Supplier Evaluation and Monitoring Procedure (QMS.7.4.1 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Supplier Evaluation and Monitoring Procedure 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…
ISO 13485:2016 QMS Template – Supplier Approval, On-boarding, Evaluation, and Monitoring Spreadsheet (QMS.7.4.1.1 – LQR) Enhance your Quality Management System with our ISO 13485:2016 compliant Supplier Approval, On-boarding, Evaluation, and Monitoring Spreadsheet, expertly crafted by the professionals at Patient Guard. Our Medical Device Quality Assurance and Regulatory Affairs document templates are developed by experienced experts,…
ISO 9001:2015 QMS Template – Supplier Evaluation and Monitoring (QMS.8.4.1 – QP) Enhance your Quality Management System with our ISO 9001:2015 compliant Supplier Evaluation and Monitoring template. Created by the fully qualified and experienced professionals at Patient Guard, this template meets the specific requirements of each clause and section of the ISO 9001:2015 standard. Why…
ISO 9001:2015 QMS Template – Supplier Evaluation Form (QMS.8.4.1.2 – QT) Enhance your Quality Management System with our ISO 9001:2015 compliant Supplier Evaluation Form template. Created by the fully qualified and experienced professionals at Patient Guard, this template meets the specific requirements of each clause and section of the ISO 9001:2015 standard. Why Choose Our…
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