Freyr’s Comprehensive toolkit is designed to equip your medical device company with all mandatory ISO 13485:2016 requirements. This comprehensive package includes documents (Procedures included ) which will facilitate your medical device company to streamline and establish all your quality management system as per ISO13485:2016.

Key Features
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End to end Solution
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Customisable Toolkit
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Includes 90+ Templates and Procedures
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Cost Efficient




