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European Medicines Agency (EMA)
Article 87

Article 87

1.
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).
2.
Where reference is made to this paragraph, Article 5 of Regulation (EU) No 182/2011 shall apply.
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