Showing 33–48 of 121 results
ISO 13485:2016 QMS Template – Document Control Procedure (QMS.4.2.4 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Document Control 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 – Employee Induction Form (QMS.6.2.0.1 – QR) Enhance your Quality Management System with our ISO 13485:2016 compliant Employee Induction Form 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 9001:2015 QMS Template – Employee Induction Template (QMS.7.2.1 – QT) Enhance your Quality Management System with our ISO 9001:2015 compliant Employee Induction 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 Employee…
ISO 13485:2016 QMS Template – Feedback & Complaints Spreadsheet (QMS.8.2.2.1 – QR) Enhance your Quality Management System with our ISO 13485:2016 compliant Feedback & Complaints Spreadsheet 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 – Feedback Procedure (QMS.8.2.1 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Feedback 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…
ISO 9001:2015 QMS Template – Feedback Procedure (QMS.9.1.2 – QP) Enhance your Quality Management System with our ISO 9001:2015 compliant Feedback Procedure 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 Feedback Procedure…
ISO 13485:2016 QMS Template – Goods In, Goods Out & Preservation of Product Procedure (QMS.7.4.3 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Goods In, Goods Out & Preservation of Product Procedure template, expertly crafted by the professionals at Patient Guard. Our Medical Device Quality Assurance and Regulatory Affairs document templates…
General Safety & Performance Requirements (GSPR) Checklist Template IVDR 2017 746 The General Safety and Performance Requirements (GSPR) checklist is a checklist against Annex I of the In Vitro Diagnostic Device Regulations (IVDR) EU 2017 746. The device needs to be assessed against each clause of annex I, and evidence presented on how the requirements…
ISO 13485 – GSPR Checklist Template MDR 2017 745 Enhance your compliance with the Medical Device Regulations (MDR) EU 2017 745 using our comprehensive General Safety and Performance Requirements (GSPR) checklist template. This template aligns with Annex I of the MDR, ensuring your device meets all necessary clauses. Key Features of Our GSPR Checklist Template:…
ISO 13485:2016 QMS Template – Infrastructure, Work Environment & Contamination Control (QMS.6.3.0 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Infrastructure, Work Environment & Contamination Control 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 Templates – Internal Audit Bundle Enhance your Quality Management System with our ISO 13485:2016 compliant Internal Audit document templates, 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…
ISO 13485:2016 QMS Template – Internal Audit Plan & Checklist (QMS.8.2.4.2 – QR) Enhance your Quality Management System with our ISO 13485:2016 compliant Internal Audit Plan & Checklist 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 9001:2015 QMS Template – Internal Audit Plan (QMS.9.2.2 – QR) Enhance your Quality Management System with our ISO 9001:2015 compliant Internal Audit Plan 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…
ISO 13485:2016 QMS Template – Internal Audit Procedure (QMS.8.2.4 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Internal Audit 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 9001:2015 QMS Template – Internal Audit Procedure (QMS.9.2 – QP) Enhance your Quality Management System with our ISO 9001:2015 compliant Internal Audit Procedure 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…
ISO 13485:2016 QMS Template – Internal Audit Report (QMS.8.2.4.3 – QR) Enhance your Quality Management System with our ISO 13485:2016 compliant Internal Audit Report 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…
End of content
End of content
No products in the cart.
