{"id":344,"date":"2018-05-29T08:20:09","date_gmt":"2018-05-29T08:20:09","guid":{"rendered":"https:\/\/az.research.umich.edu\/medschool\/glossary\/medschool-glossary-external-adverse-event\/"},"modified":"2024-11-19T22:29:10","modified_gmt":"2024-11-19T22:29:10","slug":"external-adverse-event","status":"publish","type":"glossary","link":"https:\/\/az.research.umich.edu\/medschool\/glossary\/external-adverse-event\/","title":{"rendered":"External Adverse Event"},"template":"","class_list":["post-344","glossary","type-glossary","status-publish","hentry"],"acf":{"glossary_term_description":"<p>From the perspective of an Investigator engaged in a multicenter clinical trial, external adverse events are those adverse events experienced by subjects enrolled by investigators at other institutions engaged in the clinical trial (not under IRBMED authority).<\/p>","glossary_related_terms":"","legacy_glossary_node_id":574,"legacy_related_terms":""},"_links":{"self":[{"href":"https:\/\/az.research.umich.edu\/medschool\/wp-json\/wp\/v2\/glossary\/344","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/az.research.umich.edu\/medschool\/wp-json\/wp\/v2\/glossary"}],"about":[{"href":"https:\/\/az.research.umich.edu\/medschool\/wp-json\/wp\/v2\/types\/glossary"}],"wp:attachment":[{"href":"https:\/\/az.research.umich.edu\/medschool\/wp-json\/wp\/v2\/media?parent=344"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}