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Quality Assurance and Regulatory Affairs consultancy for medical device manufacturers, suppliers and distributors based in Belgium. Specialized in implementing ISO 13485:2016, FDA QSR and EU MDR as well as gaining market authorization in Europe or US.

Company’s Keywords:

medical devices, eu mdr, regulatory affairs, iso 134852016, ce marking, fda, quality assurance

Q How Many Employees Does This Company Have?

<1

Q Which Industry Does This Company Belong To?

Q What Is the Annual Income?

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Q What Is the Technology of All the Company’s Website?

Q What Year Was the Company Founded?

<2017

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