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European Medicines Agency (EMA)
Article 87

Article 87

The Commission shall be assisted by the Standing Committee on Medicinal Products for Human Use established by Article 121 of Directive 2001/83/EC. That committee shall be a committee within the meaning of Regulation (EU) No 182/2011 of the European Parliament and of the Council (9).
Where reference is made to this paragraph, Article 5 of Regulation (EU) No 182/2011 shall apply.