Statutory Instruments

The European Communities (Clinical Trials on Medicinal Products for Human Use) (Amendment) Regulations 2004 – S.I. No. 878 of 2004

These Regulations make provision for the payment of charges for services provided by the Irish Medicines Board in respect of clinical trials conducted under the European Communities ( Clinical Trials on Medicinal Products for Human Use ) Regulations 2004 ( S.I. No. 190 of 2004 ). The charges are determined by the Irish Medicines Board subject
to the approval of the Minister for Health and Children

S.I. no. 878 of 2004