Supplier Management Procedure | ISO 13485 | FDA QSR Compliant
SKU: SOP 7-006
The ISO 13485 Supplier Management Procedure governs the review, approval and continuous monitoring of all suppliers to ensure conformance to regulatory requirements.
- ISO 13485:2016 Compliant
- FDA QSR Compliant
- Includes Related Forms
- MS Word Format
- Digital Content - Instant Download
ISO 13485 Supplier Management Procedure
The ISO 13485 supplier management procedure establishes a process to ensure that suppliers of products, components and services conform to regulatory requirements.
ISO 13485 Supplier Management Overview
The ISO 13485 supplier management procedure measures, reviews and qualifies suppliers based upon their ability to produce a product, component, or service that considers associated risks.
The ISO 13485 Supplier Management Procedure includes supplier review and assessment forms, performance measurement data forms and the internal processes used to establish an approved supplier.
ISO 13485 Supplier Management Procedure Compliance
The Supplier Management Procedure is ISO 13485:2016 and FDA 21 CFR Part 820 compliant.
To learn more about our ISO 13485 Supplier Management Procedure contact us at firstname.lastname@example.org
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