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English
$
USD
Saudi Arabia
4 orders completed
Quality Assurance, Regulatory and Customer Support, Procurement
I prepare the Quality Manual for Medical Device Company following ISO 13485:2016 especially for the companies who need to be certified and enable to sell,store and distribute medical devices with approval from regulatory authorities e.g FDA, USFA, EU etc. I have worked out the quality manual templates for GCC regions, (SFDA)
Document type:
User & training manuals
•
Documentation
Language:
English
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