Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Safety_monitoring> ?p ?o }
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- Safety_monitoring abstract "Safety monitoring of a clinical trial is conducted by an independent physician with relevant expertise. This is accomplished by review of adverse event, immediately after they occur, with timely follow-up through resolution. Responsibility for data and safety monitoring depends on the phase of the study and may be conducted by sponsor or Contract research organization (CRO) staff or contractor, and/or by the Principal clinical investigator/project manager conducting the study. Regardless of the method used, monitoring must be performed on a regular basis. Oversight of the monitoring activity is the responsibility of the sponsor.".
- Safety_monitoring wikiPageExternalLink www.clinicaltrials.gov.
- Safety_monitoring wikiPageExternalLink www.fda.gov.
- Safety_monitoring wikiPageExternalLink 503_trial.html.
- Safety_monitoring wikiPageExternalLink www.ibpassociation.org.
- Safety_monitoring wikiPageExternalLink ibpa_unpublished_articles.htm.
- Safety_monitoring wikiPageExternalLink www.ich.org.
- Safety_monitoring wikiPageID "2234530".
- Safety_monitoring wikiPageLength "1646".
- Safety_monitoring wikiPageOutDegree "13".
- Safety_monitoring wikiPageRevisionID "648449564".
- Safety_monitoring wikiPageWikiLink Adverse_event.
- Safety_monitoring wikiPageWikiLink Category:Clinical_research.
- Safety_monitoring wikiPageWikiLink Category:Medical_monitoring.
- Safety_monitoring wikiPageWikiLink Category:Pharmaceutical_industry.
- Safety_monitoring wikiPageWikiLink Clinical_investigator.
- Safety_monitoring wikiPageWikiLink Clinical_trial.
- Safety_monitoring wikiPageWikiLink Contract_research_organization.
- Safety_monitoring wikiPageWikiLink Data_monitoring_committee.
- Safety_monitoring wikiPageWikiLink European_Medicines_Agency.
- Safety_monitoring wikiPageWikiLink Food_and_Drug_Administration.
- Safety_monitoring wikiPageWikiLink Monitoring_in_clinical_trials.
- Safety_monitoring wikiPageWikiLink Serious_adverse_event.
- Safety_monitoring wikiPageWikiLink United_States_National_Library_of_Medicine.
- Safety_monitoring wikiPageWikiLinkText "Safety monitoring".
- Safety_monitoring wikiPageWikiLinkText "safety monitoring".
- Safety_monitoring wikiPageUsesTemplate Template:Pharma-stub.
- Safety_monitoring subject Category:Clinical_research.
- Safety_monitoring subject Category:Medical_monitoring.
- Safety_monitoring subject Category:Pharmaceutical_industry.
- Safety_monitoring type Industry.
- Safety_monitoring type Pharmaceutic.
- Safety_monitoring comment "Safety monitoring of a clinical trial is conducted by an independent physician with relevant expertise. This is accomplished by review of adverse event, immediately after they occur, with timely follow-up through resolution. Responsibility for data and safety monitoring depends on the phase of the study and may be conducted by sponsor or Contract research organization (CRO) staff or contractor, and/or by the Principal clinical investigator/project manager conducting the study.".
- Safety_monitoring label "Safety monitoring".
- Safety_monitoring sameAs Q7398657.
- Safety_monitoring sameAs m.06y1vc.
- Safety_monitoring sameAs Q7398657.
- Safety_monitoring wasDerivedFrom Safety_monitoring?oldid=648449564.
- Safety_monitoring isPrimaryTopicOf Safety_monitoring.