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CE Marking of Medical Devices or a product's is used for compliance with the valid for EU regulations and European countries. A CE Mark Consultants file is an all-inclusive description file of your device planned to display fulfillment with European requirements. We offer limitless manufacturers understand and meet the requirements of applicable Medical Device CE Marking. For more information about our services, visit our website. http://www.i-3-c.com/
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I3C or QARA provides online service for ISO 13485:2016 for medical devices and QMS (quality management systems). Contact us online for ISO 13485 Certi...
Quality Solutions – Pharma, Food & cosmetics Consultancy services at Navi Mumbai Training on GMP , GLP, Validation, QA/QC, Production – Manufa...