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The person responsible for regulatory compliance in the medical device law and its liability

This article shall – after a quick introduction into the European Medial Device Regulation –
examine the duties of the so called „person responsible for regulatory compliance“ of medical device
manufacturers.

Identiferoai:union.ndltd.org:DRESDEN/oai:qucosa:de:qucosa:91369
Date14 May 2024
CreatorsRenz, Christoph
Source SetsHochschulschriftenserver (HSSS) der SLUB Dresden
LanguageEnglish
Detected LanguageEnglish
Typeinfo:eu-repo/semantics/publishedVersion, doc-type:article, info:eu-repo/semantics/article, doc-type:Text
Rightsinfo:eu-repo/semantics/openAccess
Relationurn:nbn:de:bsz:15-qucosa2-913641, qucosa:91364

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