Third Party Regulatory Information Submitter

Preferred Label : Third Party Regulatory Information Submitter;

NCIt related terms : Third Party;

NCIt definition : An outside party delegated to submit regulatory information.;

Alternative definition : FDA: The third party delegated by a manufacturer to submit regulatory information on behalf of a manufacturer of medical devices.;

Détails

Origin ID

C101710;

UMLS CUI

C3539931;

Semantic type(s)
- Professional or Occupational Group [UMLS semantic type]
concept_is_in_subset
- FDA CDRH GUDID Terminology [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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