Showing 17–32 of 121 results
ISO 9001:2015 QMS Template – Continual Improvement Tracker (QMS.10.3 – QR) Elevate your Quality Management System with our ISO 9001:2015 compliant Continual Improvement Tracker 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 – Control of Creating & Updating Records (QMS.7.5.2 – QP) Enhance your Quality Management System with our ISO 9001:2015 compliant Control of Creating & Updating Records template, expertly crafted by the professionals at Patient Guard. Our Quality Assurance and Regulatory Affairs document templates are developed by experienced experts, ensuring they meet…
ISO 9001:2015 QMS Template – Control of Documented Information (QMS.7.5.3 – QP) Elevate your Quality Management System with our ISO 9001:2015 compliant Control of Documented Information template, crafted by the experts at Patient Guard. Our Quality Assurance and Regulatory Affairs document templates are meticulously developed by seasoned professionals, ensuring they meet every clause and section…
ISO 9001:2015 QMS Template – Control of Measurement and Monitoring of Equipment (QMS.7.1.5.1- QP) Elevate your Quality Management System with our ISO 9001:2015 compliant Control Measurement and Monitoring of Equipment template, expertly crafted by the professionals at Patient Guard. Our Quality Assurance and Regulatory Affairs document templates are developed by experienced experts, ensuring they meet…
ISO 13485:2016 QMS Template – Control Measurement and Monitoring Equipment Procedure (QMS.7.6.0 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Control Measurement and Monitoring Equipment 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 9001:2015 QMS Template – Control of Production and Service Provision (QMS.8.5.1 – QP) Elevate your Quality Management System with our ISO 9001:2015 compliant Control of Production and Service Provision template, crafted by the experts at Patient Guard. Our Quality Assurance and Regulatory Affairs document templates are meticulously developed by seasoned professionals, ensuring they meet…
ISO 13485:2016 QMS Template – Control of Records Procedure (Q.M.S.4.2.5) Enhance your Quality Management System with our ISO 13485:2016 compliant Control of Records 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…
EU and UK Cosmetic Product Information File (PIF) Template When selling cosmetic products in the EU or UK markets, you must create a Product Information File (PIF) for each product and its variants. The PIF proves your products comply with cosmetics regulations EC No 1223 2009. Without a complete PIF, you cannot legally sell your…
ISO 9001:2015 QMS Template – Customer Related Processes (QMS.8.2.1 – QP) Enhance your Quality Management System with our ISO 9001:2015 compliant Customer Related Processes 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 – Customer Related Processes Procedure (QMS.7.2.0 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Customer Related Processes 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…
Declaration of Conformity Template – IVDR 2017 746 The declaration of conformity is a statement made and signed by the legal manufacturer that they have met all the regulatory requirements stated within the regulation. This template meets the required information needed on a declaration of conformity to medical device regulation EU 2017 746. The Declaration of Conformity…
Declaration of Conformity Template – MDR 2017 745 The declaration of conformity is a statement made and signed by the legal manufacturer that they have met all the regulatory requirements stated within the regulation. This template meets the required information needed on a declaration of conformity to medical device regulation EU 2017 745. If you…
The declaration of conformity is a statement made and signed by the legal manufacturer that they have met all the regulatory requirements stated within the regulation. This template meets the required information needed on a declaration of conformity to the UK Medical Device Regulations 2002. If you would like further information on our wide range…
ISO 13485:2016 QMS Template – Design and Development Procedure (QMS.7.3.0 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Design and Development 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 9001:2015 QMS Template – Design and Development Procedure (QMS.8.3.2 – QP) Enhance your Quality Management System with our ISO 9001:2015 compliant Design and Development 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…
ISO 13485:2016 QMS Template – Device History Record (QMS.7.5.1 – QP) Enhance your Quality Management System with our ISO 13485:2016 compliant Device History 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 they meet the specific requirements of…
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