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The STAR Compass to Guide Future Pharmacovigilance Based on a 10-Year Review of the Strengthened EU System.
Bahri, Priya; Genov, Georgy; Arlett, Peter; Sarinic, Viola Macolic; Korakianiti, Evdokia; Nolte, Alexis; Huber, Martin; Straus, Sabine M J M.
Affiliation
  • Bahri P; European Medicines Agency (EMA), Domenico Scarlattilaan 6, 1083 HS, Amsterdam, The Netherlands. priya.bahri@ema.europa.eu.
  • Genov G; European Medicines Agency (EMA), Domenico Scarlattilaan 6, 1083 HS, Amsterdam, The Netherlands.
  • Arlett P; European Medicines Agency (EMA), Domenico Scarlattilaan 6, 1083 HS, Amsterdam, The Netherlands.
  • Sarinic VM; European Medicines Agency (EMA), Domenico Scarlattilaan 6, 1083 HS, Amsterdam, The Netherlands.
  • Korakianiti E; European Medicines Agency (EMA), Domenico Scarlattilaan 6, 1083 HS, Amsterdam, The Netherlands.
  • Nolte A; European Medicines Agency (EMA), Domenico Scarlattilaan 6, 1083 HS, Amsterdam, The Netherlands.
  • Huber M; Federal Institute for Drugs and Medical Devices, Bonn, Germany.
  • Straus SMJM; EMA Pharmacovigilance and Risk Assessment Committee, Amsterdam, The Netherlands.
Drug Saf ; 47(10): 941-956, 2024 Oct.
Article de En | MEDLINE | ID: mdl-38987419
ABSTRACT
This article reflects on the 2010 pharmacovigilance legislation of the European Union (EU). Its legislative aim of better patient and public health protection through new responsibilities for pharmaceutical companies and regulatory bodies is considered to have been achieved and is well supported by the good pharmacovigilance practices 'EU-GVP'. For future progress, we set out a vision for high-quality pharmacovigilance in a world of ongoing medical, technological and social changes. To deliver this vision, four principles are proposed to guide actions for further progressing the EU pharmacovigilance system synergistic interactions with healthcare systems; trustworthy evidence for regulatory decisions; adaptive process efficiency; and readiness for emergency situations (the 'STAR principles'). Like a compass, these principles should guide actions for building capacity, technology and methods; improving regulatory processes; and expanding policies, frameworks and research agendas. Fit for the future, the EU system should achieve further improved outputs in terms of safe, effective and trusted use of medicines and positive health outcomes within patient-centred healthcare.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Systèmes de signalement des effets indésirables des médicaments / Union européenne / Pharmacovigilance Limites: Humans Langue: En Journal: Drug Saf Sujet du journal: TERAPIA POR MEDICAMENTOS / TOXICOLOGIA Année: 2024 Type de document: Article Pays d'affiliation: Pays-Bas Pays de publication: Nouvelle-Zélande

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Systèmes de signalement des effets indésirables des médicaments / Union européenne / Pharmacovigilance Limites: Humans Langue: En Journal: Drug Saf Sujet du journal: TERAPIA POR MEDICAMENTOS / TOXICOLOGIA Année: 2024 Type de document: Article Pays d'affiliation: Pays-Bas Pays de publication: Nouvelle-Zélande