| Literature DB >> 30222390 |
Paulami Naik1,2, Thomas Umrath3, John van Stekelenborg4, Regina Ruben5,2, Nasiba Abdul-Karim6, Robert Boland7, Michael Ibara8,2, Jethro Ekuta4, Dana Washburn9, Stella Stergiopoulos1.
Abstract
Social media presents new challenges to the biopharmaceutical industry for conducting pharmacovigilance activities. The authors reviewed worldwide regulatory guidance documents related to monitoring of adverse events posted on social media sites and identified gaps in current regulatory definitions for pharmacovigilance. Points to consider for addressing these gaps are made to offer standards for industry consideration and a potential framework for guidance from global health authorities.Keywords: adverse events on social media; drug safety; pharmacovigilance; regulatory harmonization; social media monitoring
Year: 2015 PMID: 30222390 DOI: 10.1177/2168479015587362
Source DB: PubMed Journal: Ther Innov Regul Sci ISSN: 2168-4790 Impact factor: 1.778