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EU MDR Art. 1(8), 1(9), 117 · Directive 2001/83/EC · 21 CFR Parts 3 and 4 Drug-Device Combination Products: EU MDR and FDA Requirements Both systems, from qualification to post-market — every requirement stated with its article, and the document each one obliges you to hold. €339 VAT calculated at checkout Get the course 27…
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