The Medicines for Human Use (Clinical Trials) and Blood Safety and Quality (Amendment) Regulations 2008
1Citation, commencement and interpretation
2Amendment of regulation 2 of the Clinical Trials Regulations
3Amendment of regulation 15 of the Clinical Trials Regulations
4Amendment of Schedule 1 to the Clinical Trials Regulations
5Amendment of Schedule 2 to the Clinical Trials Regulations
6Amendment of Schedule 3 to the Clinical Trials Regulations
7Amendment of regulation 7 of the Blood Regulations
8Amendment of regulation 8 of the Blood Regulations
9Amendment of regulation 12B of the Blood Regulations
2008 No. 941
Medicines

The Medicines for Human Use (Clinical Trials) and Blood Safety and Quality (Amendment) Regulations 2008

Made
Laid before Parliament
Coming into force
The Secretary of State makes the following Regulations in exercise of the powers conferred upon him by section 2(2) of the European Communities Act 19721. He has been designated for the purposes of that section in relation to medicinal products2 and in relation to health protection measures regulating the use of material of human origin3.