Master Document List Template - ISO 9001
Master Document List Template - ISO 9001
Template Overview
Template Overview
Maintain full control over your Quality Management System (QMS) documentation with our ISO 9001:2015 Clause 7.5 Master Document List Template. Proper document control is essential for ensuring consistency, traceability, and compliance with ISO 9001:2015 standards. This ready-to-use template provides a structured framework to organize, track, and manage all controlled documents within your organization, ensuring they are up to date, approved, and easily accessible.
Key Features
Key Features
✔ Pre-Formatted Master Document List – Covers key ISO 9001:2015 Clause 7.5 requirements.
✔ Document Identification & Version Control – Track document numbers, titles, revision history, and approval status.
✔ Approval & Review Workflow – Assign responsibilities for document verification and periodic review.
✔ Storage & Access Control Guidelines – Ensure secure storage, retrieval, and controlled distribution.
✔ Obsolete Document Management – Define procedures for handling outdated or replaced documents.
✔ Audit-Ready Documentation & Compliance Tracking – Maintain structured records for internal audits and regulatory inspections.
✔ Editable Digital Format – Fully customizable for various industries and business models.
Why choose a QMS Template?
Why choose a QMS Template?
This master document list template is ideal for quality managers, compliance officers, and document control teams, ensuring a structured, compliant, and effective document management system.
Download the ISO 9001:2015 Master Document List Template today and enhance your document control and compliance strategy!
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Additional information
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About Patient Guard
QMSRegs was founded in 2020 by the Patient Guard group to help companies get their medical devices to market and achieve Medical Device compliance. Patient Guard’s consultancy services offers a cost-effective solution for all your Quality Management System needs.
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Contact Us
For more templates and services in Medical Device Quality Assurance and Regulatory Affairs, or to provide feedback, contact us at qmsregs@patientguard.com.