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• W1520666503 abstract "Pharmacoepidemiology and Drug SafetyVolume 23, Issue 1 p. 105-105 Letter to the Editor Critically reviewing impact of regulatory actions, not just FDA's Peter G. M. Mol, Peter G. M. Mol Department of Clinical Pharmacology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands Dutch Medicines Evaluation Board, Utrecht, The NetherlandsSearch for more papers by this author Peter G. M. Mol, Peter G. M. Mol Department of Clinical Pharmacology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands Dutch Medicines Evaluation Board, Utrecht, The NetherlandsSearch for more papers by this author First published: 03 January 2014 https://doi.org/10.1002/pds.3509Citations: 1 E-mail: [email protected] Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES 1 Briesacher BA, Soumerai SB, Zhang F, et al. A critical review of methods to evaluate the impact of FDA regulatory actions. Pharmacoepidemiol Drug Saf 2013. DOI: 10.1002/pds.3480 2 The European Parliament and the European Council. REGULATION (EU) No 1235/2010 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL, 2010. http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2010:348:0001:0016:EN:PDF 3 The European Parliament and the European Council. DIRECTIVE 2010/84/EU OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL, 2010. http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2010:348:0074:0099:EN:PDF 4 Piening S, Haaijer-Ruskamp FM, de Vries JT, et al. Impact of safety-related regulatory action on clinical practice: a systematic review. Drug Saf 2012; 35(5): 373–385. 5 Mol PG, Straus SM, Piening S, de Vries JT, de Graeff PA, Haaijer-Ruskamp FM. A decade of safety-related regulatory action in the Netherlands: a retrospective analysis of direct healthcare professional communications from 1999 to 2009. Drug Saf 2010; 33(6): 463–474. 6 Reber KC, Piening S, Wieringa JE, et al. When direct health-care professional communications have an impact on inappropriate and unsafe use of medicines. Clin Pharmacol Ther 2013; 93(4): 360–365. 7 Wood AJ. If you don't know where you are going, you can't tell if you have arrived: defining goals for drug safety announcements. Clin Pharmacol Ther 2013; 93(4): 302–303. 8 Prieto L, Spooner A, Hidalgo-Simon A, Rubino A, Kurz X, Arlett P. Evaluation of the effectiveness of risk minimization measures. Pharmacoepidemiol Drug Saf 2012; 21(8): 896–899. Citing Literature Volume23, Issue1January 2014Pages 105-105 ReferencesRelatedInformation" @default.
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