These Regulations may be cited as the Good Laboratory Practice (Codification Amendments Etc.) Regulations 2004 and shall come into force on 27th April 2004.
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The Good Laboratory Practice (Codification Amendments Etc.) Regulations 2004
The Good Laboratory Practice Regulations 1999 are amended as follows:—
(a) in regulation 2 (interpretation), in paragraph (1)—
(i) for the definition of “principles of good laboratory practice” there is substituted the following definition—
“principles of good laboratory practice” means—
the principles of good laboratory practice set out in Schedule 1, which are based on the Good Laboratory Practice Principles set out in Section II of Annex I to the European Parliament and Council Directive 2004/10/ EC on the harmonisation of laws, regulations and administrative provisions relating to the application of the principles of good laboratory practice and the verification of their applications for tests on chemical substances; read with
the revised guidance for the conduct of test facility inspections and study audits set out in Schedule 2, which is based on part of the Revised Guidance for the Conduct of Test Facility Inspections and Study Audits in Annex I to the European Parliament and Council Directive 2004/9/EC on the inspection and verification of good laboratory practice;
(ii) in the definition of “regulatory studies”, at the start of paragraph (c) there is inserted “in respect of which”;
(b) in regulation 5 (prospective membership of the United Kingdom good laboratory practice compliance programme), in paragraph (4) the word “that” is omitted;
(c) in regulation 9 (powers of entry etc. ), in paragraph (6) for “the Annex to Council Directive 88/320/ EEC on the inspection and verification of good laboratory practice ( GLP ), as amended by Commission Directive 1999/12/EC adapting to technical progress for the second time the annex to Council Directive 88/320/EEC ” there is substituted “Annex I to the European Parliament and Council Directive 2004/9/EC ”;
(d) in Schedule 1 (good laboratory practice principles), in the heading for “(BASED ON SECTION II OF THE ANNEX TO COUNCIL DIRECTIVE 87/18/EEC , AS AMENDED BY COMMISSION DIRECTIVE 1999/11/EC )” there is substituted “(BASED ON SECTION II OF ANNEX I TO THE EUROPEAN PARLIAMENT AND COUNCIL DIRECTIVE 2004/10/EC )”;
(e) in Schedule 2 (revised guidance for the conduct of test facility inspections and study audits), in the heading for “(BASED ON PART OF PART B OF THE ANNEX TO COUNCIL DIRECTIVE 88/320/EEC , AS AMENDED BY COMMISSION DIRECTIVE 1999/12/EC )” there is substituted “(BASED ON PART OF PART B OF ANNEX I TO THE EUROPEAN PARLIAMENT AND COUNCIL DIRECTIVE 2004/9/EC )”.
In Schedule 1 (funded operations) of the Medicines and Healthcare Products Regulatory Agency Trading Fund Order 2003 for “Council Directive 87/18/EEC of 18th December 1986 as amended and Council Directive 88/320/EEC of 9th June 1988 as amended” there is substituted “the European Parliament and Council Directive 2004/10/EC of 11th February 2004 and the European Parliament and Council Directive 2004/9/EC of 11th February 2004”.
In regulation 9 (product information) of the Cosmetic Products (Safety) Regulations 2003 , in paragraph (2) for “Article 1 of Council Directive 87/18/EEC ” there is substituted “Article 1 of the European Parliament and Council Directive 2004/10/EC ”.
In regulation 2 (interpretation) of the Notification of New Substances Regulations 1993 , in paragraph (1) in the definition of “principles of good laboratory practice” for “the Good Laboratory Practice Regulations 1997” there is substituted “the Good Laboratory Practice Regulations 1999”.
Cite this legislation
The Good Laboratory Practice (Codification Amendments Etc.) Regulations 2004 (legislation.gov.uk, OGL v3.0). Retrieved via LawPlayer, https://lawplayer.com/uk/act/uksi-2004-994
Contains public sector information licensed under the Open Government Licence v3.0.
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