№ lp_1_08388
The document outlines the minimum requirements for external suppliers performing process validation on Philips’s parts, sub-assemblies, and products, aligned with international standards like ISO 13485.
Year: 2004
Region / City: International
Topic: Process Validation, Medical Device Manufacturing
Document Type: Guideline
Organization / Institution: Philips
Author: Philips Quality Engineering
Target Audience: External suppliers, manufacturers of medical devices
Effective Period: Not specified
Approval Date: Not specified
Modification Date: Not specified
Price: 8 / 10 USD
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