ISO 13485 (Clause 7.4) - Quality Inspection Plan Goods in (Supplier Name) Template
ISO 13485 (Clause 7.4) - Quality Inspection Plan Goods in (Supplier Name) Template
Template Overview
Template Overview
Ensure compliance with ISO 13485:2016 Clause 7.4 – Purchasing by implementing a structured Goods In Quality Inspection process. This Quality Inspection – Goods In Template helps medical device manufacturers verify that incoming raw materials, components, and products meet regulatory, quality, and safety requirements before being used in production.
Key Features
Key Features
✔ Pre-Formatted Quality Inspection Checklist – Covers key ISO 13485:2016 Clause 7.4 requirements.
✔ Supplier & Product Identification Sections – Ensure traceability of materials.
✔ Acceptance Criteria & Inspection Guidelines – Define pass/fail requirements for incoming goods.
✔ Packaging & Labeling Verification – Ensure materials meet regulatory and storage requirements.
✔ Defects & Non-Conformity Reporting Section – Identify and document issues for supplier communication.
✔ Traceability & Documentation Requirements – Maintain full compliance for audits and regulatory reviews.
✔ Editable Digital Format – Fully customizable for different medical devices and supplier materials.
Why choose a QMS Template?
Why choose a QMS Template?
This user-friendly template is essential for quality control teams, warehouse staff, and regulatory personnel, ensuring consistent, compliant, and efficient incoming goods inspection.
Download the ISO 13485:2016 Quality Inspection – Goods In Template today and improve your supply chain quality management!
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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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For more templates and services in Medical Device Quality Assurance and Regulatory Affairs, or to provide feedback, contact us at qmsregs@patientguard.com.