UK Parliament / Open data

Medicines for Human Use (Marketing Authorisations etc.) Amendment Regulations 2008

Statutory instrument laid in the House of Lords and House of Commons, on Monday, 8 December 2008. It was made on Wednesday, 3 December 2008.

SI 2008/3097. (Negative instrument). Together with an explanatory memorandum from the Department of Health. Coming into force 29 December 2008. Explanatory memorandum withdrawn and replaced 10 December 2008 (UP 60 2008-09).

About this statutory instrument

Reference

SI 2008/3097

Session

2008-09

Coming into force

Monday, 29 December 2008

Procedure

Negative

Medicines for Human Use (Marketing Authorisations Etc) Regulations 1994
Friday, 9 December 1994
Statutory instruments
House of Lords
House of Commons

Medicines for Human Use (Prescribing by EEA Practitioners) Regulations 2008
Wednesday, 2 July 2008
Statutory instruments
House of Lords
House of Commons

Regulation (EC) 1901/2006 of the European Parliament and of the Council on medicinal products for paediatric use and amending Regulation (EEC)1768/92, Directive 2001/20/EC, Directive 2001/83/EC and Regulation (EC)726/2004. Adopted 12 December 2006.
Wednesday, 27 December 2006
European material produced by EU institutions

Council Regulation (EEC) 1768/92 concerning the creation of a supplementary protection certificate for medicinal products. Adopted 18. 6.92.
Wednesday, 1 July 1992
European material produced by EU institutions

Show all related items (7)

European Parliament and Council Directive 2001/83/EC on Community code relating to medicinal products for human use. Adopted 06.11.2001.
Wednesday, 28 November 2001
European material produced by EU institutions

European Parliament and Council Directive 2001/20/EC on the approximation of provisions laid down by law, regulation and administrative action relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use. Adopted 04.04.2001.
Monday, 30 April 2001
European material produced by EU institutions

European Parliament and Council Regulation (EC)726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency [Agency for the Evaluation of Medicinal Products]. Adopted 31 March 2004.
Thursday, 29 April 2004
European material produced by EU institutions