Abstract
In line with increasing calls of transparency initiatives across European institutions, the European Medicines Agency (EMA) will on September 26th 2017 host its first public hearing on the regulatory of a drug, namely Valproate. According to the EMA website, the public hearing is intended to “increase transparency by opening up the scientific evaluation process” and “[give citizens] a voice in the evaluation of medicines.” This conference paper will present the preliminary results from a rhetorical analysis of the public hearing as a transparency measure. What kind transparency does a public hearing provide? How are citizens’ accounts positioned vis-à-vis expert testimonies? Does the public hearing achieve sufficient “hybridity” of its heterogeneous stakeholder group?
Original language | English |
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Publication date | 2 Oct 2017 |
Publication status | Published - 2 Oct 2017 |