Compare ISO 9001 and ISO 13485
ISO 13485 differs from 9001 in several areas critical to the Medical Device industry:- From QMS Continuous Improvement to maintaining the effectiveness (since it must meet certain requirements as a medical device)
- Focus on meeting regulatory requirements versus increasing customer satisfaction.
- Additional documentation requirements (depending on product) including
- Regulatory requirements
- Health, cleanliness, sterilization
- Risk management
- Purchased material for traceability
- Labeling and packaging
- etc.
Compare of the requirements of ISO 9001 and ISO 13485
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