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The Medicines for Human Use (Clinical Trials) Regulations 2004

The Medicines for Human Use (Clinical Trials) Regulations 2004

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amended(d); “doctor” means a registered medical practitioner(e); “EEA State” means a State which is a Contracting Party to the EEA Agreement; “EEA Agreement” means the Agreement on the European Economic Area signed at Oporto on 2nd May 1992(f) as adjusted by the Protocol signed at Brussels on 17th March 1993(g);

  Protocol, Amended, Brussels

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