Knowledge of Adverse Drug Reaction Reporting and the Pharmacovigilance of Biological Medicines: A Survey of Healthcare Professionals in Ireland

Background In Europe, changes to pharmacovigilance legislation, which include additional monitoring of medicines, aim to optimise adverse drug reaction (ADR) reporting systems. The legislation also makes provisions related to the traceability of biological medicines. Objective The objective of this...

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Veröffentlicht in:	BioDrugs : clinical immunotherapeutics, biopharmaceuticals, and gene therapy biopharmaceuticals, and gene therapy, 2018-06, Vol.32 (3), p.267-280
Hauptverfasser:	O’Callaghan, J., Griffin, B. T., Morris, J. M., Bermingham, Margaret
Format:	Artikel
Sprache:	eng
Schlagworte:	Antibodies Biological products Biomedical and Life Sciences Biomedicine Brand names Cancer Research Hospitals Knowledge Legislation Manufacturing Marketing Medicine Molecular Medicine Nurses Original Original Research Article Patients Pharmacotherapy Pharmacovigilance Physicians Questionnaires Systematic review
Online-Zugang:	Volltext
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