Emergo provides quality and regulatory compliance consulting to medical device and IVD companies. We assist with medical device registration/approval, regulatory strategy, ISO 13485 and QMS compliance, local in-country representation and post market surveillance in 20+ markets worldwide. Offices in North America, South America, Europe, Asia, Australia and the Middle East.
Company’s Keywords:
regulatory strategy & consulting, qms implementation & audits, medical device & ivd registation, clinical data evaluation & pmcf, incountry regulatory representation, post market surveillance consulting
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