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Françoise Schlemmer will be involved in training on the regulatory aspects of medical devices and more specifically on the impacts of the new European regulation.

090517She will address, inter alia, the implications of the new requirements for notified bodies on audits and will focus on major impacts for manufacturers.

By | 2018-06-29T11:19:15+00:00 May 8th, 2017|news|0 Comments

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