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Overview of the European post-authorisation study register post-authorization studies performed in Europe from September 2010 to December 2018.
Sultana J, Crisafulli S, Almas M, Antonazzo IC, Baan E, Bartolini C, Bertuccio MP, Bonifazi F, Capuano A, Didio A, Ehrenstein V, Felisi M, Ferrajolo C, Fontana A, Francisca R, Fourrier-Reglat A, Fortuny J, Gini R, Hyeraci G, Hoeve C, Kontogiorgis C, Isgrò V, Lalagkas PN, L'Abbate L, Layton D, Landi A, Narduzzi S, Roque Pereira L, Poulentzas G, Rafaniello C, Roberto G, Scondotto G, Sportiello L, Toma M, Toussi M, Verhamme K, Volpe E, Trifirò G; On behalf the Working Group 3 of ENCePP (Inventory of EU data sources and methodological approaches for multisource studies). Sultana J, et al. Among authors: francisca r. Pharmacoepidemiol Drug Saf. 2022 Jun;31(6):689-705. doi: 10.1002/pds.5413. Epub 2022 Feb 11. Pharmacoepidemiol Drug Saf. 2022. PMID: 35092329 Free PMC article.
EU postmarket surveillance plans for medical devices.
Pane J, Francisca RDC, Verhamme KMC, Orozco M, Viroux H, Rebollo I, Sturkenboom MCJM. Pane J, et al. Among authors: francisca rdc. Pharmacoepidemiol Drug Saf. 2019 Sep;28(9):1155-1165. doi: 10.1002/pds.4859. Epub 2019 Jul 18. Pharmacoepidemiol Drug Saf. 2019. PMID: 31318470 Free PMC article. Review.