The Medicines (Marketing Authorisations Etc.) Amendment Regulations 2005
1Citation and commencement
2Amendment of the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994
3Amendments of the Patents Act 1977
4Consequential amendments to enactments
SCHEDULEAMENDMENTS TO OTHER ENACTMENTS
1In the Medicines (Pharmacy and General Sale Exemption) Order 1980...
2In the Medicines (Applications for Grant of Product Licences –...
3In the Medical Devices (Consultation Requirements) (Fees) Regulations 1995, in...
4In the Genetically Modified Organisms (Risk Assessment) (Records and Exemptions)...
5In the Prescription Only Medicines (Human Use) Order 1997, in...
6In the Health Service Medicines (Control of Prices of Branded...
7In the Genetically Modified Organisms (Contained Use) Regulations 2000 in...
8In the Biocidal Products Regulations 2001 in regulation 3 (application),...
9In the Genetically Modified Organisms (Deliberate Release) (Scotland) Regulations 2002...
10In the Medical Devices Regulations 2002, in regulation 2 (interpretation),...
11In the Genetically Modified Organisms (Deliberate Release) Regulations 2002, in...
12In the Genetically Modified Organisms (Deliberate Release) (Wales) Regulations 2002...
13In the Food Supplements (England) Regulations 2003, in regulation 3...
14In the Food Supplements (Scotland) Regulations 2003 in regulation 3...
15In English text of the Food Supplements (Wales) Regulations 2003(Rheoliadau...
16In the National Health Service (General Medical Services Contracts) (Wales)...
17In the Medicines for Human Use (Clinical Trials) Regulations 2004,...
18In the General Product Safety Regulations 2005 in regulation 33...
19In Schedule 13 to the Enterprise Act 2002, for paragraph...
2005 No. 2759
MEDICINES

The Medicines (Marketing Authorisations Etc.) Amendment Regulations 2005

Made
Laid before Parliament
Coming into force
for the purpose of regulation 2(2)(a)(ii) and (vi) and (c),(9)(a),(11)(a),(14)(e),(f)(i),(iii) to (v) and paragraphs and 17(b) of the Schedule
For all other purposes
The Secretary of State, being a Minister designated1 for the purposes of section 2(2) of the European Communities Act 19722 in relation to medicinal products, in exercise of the powers conferred by the said section 2(2), makes the following Regulations: