- Latest available (Revised)
- Original (As made)
This is the original version (as it was originally made). Northern Ireland Statutory Rules are not carried in their revised form on this site.
Statutory Rules of Northern Ireland
FOOD
Made
2nd October 2008
Coming into operation
4th November 2008
The Department of Health, Social Services and Public Safety F1 makes the following Regulations in exercise of the powers conferred by Articles 15(1)(e), 16(1), 25(1)(a) and (3) and 47(2) of the Food Safety (Northern Ireland) Order 1991 F2.
In accordance with Article 47(3A) of the Food Safety (Northern Ireland) Order 1991, the Department of Health, Social Services and Public Safety has had regard to relevant advice given by the Food Standards Agency.
As required by Article 9 of Regulation (EC) No. 178/2002 of the European Parliament and of the Council laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety F3 there has been open and transparent public consultation during the preparation and evaluation of these Regulations.
Annotations are used to give authority for changes and other effects on the legislation you are viewing and to convey editorial information. They appear at the foot of the relevant provision or under the associated heading. Annotations are categorised by annotation type, such as F-notes for textual amendments and I-notes for commencement information (a full list can be found in the Editorial Practice Guide). Each annotation is identified by a sequential reference number. For F-notes, M-notes and X-notes, the number also appears in bold superscript at the relevant location in the text. All annotations contain links to the affecting legislation.
Amendments (Textual)
F2S.I. 1991/762 (N.I.7) as amended by S.I. 1996/1663 (N.I.12), paragraphs 26 to 42 of Schedule 5 and Schedule 6 to the Food Standards Act 1999 c.28 and S.R.2004 Nos. 482 and 505
F3OJ No. L31, 1.2.2002, p.1, as last amended by Commission Regulation (EC) No. 202/2008 amending Regulation (EC) No. 178/2002 of the European Parliament and of the Council as regards the number and names of the Scientific Panels of the European Food Safety Authority (OJ No. L60, 5.3.2008, p.17)
1. These Regulations—
(a)may be cited as the Infant Formula and Follow-on Formula (Amendment) Regulations (Northern Ireland) 2008; and
(b)come into operation on 4th November 2008.
2.—(1) The Infant Formula and Follow-on Formula Regulations (Northern Ireland) 2007 F4 are amended in accordance with paragraphs (2) to (6).
(2) For the provisions of regulation 3 (prohibition on the marketing of infant formula or follow-on formula unless certain conditions are met) substitute —
“(1) A person shall not market infant formula which contravenes regulation 5, 6, 8, 10, 11, 12, 14(1), (2) or (3), 15, 17, 19 or 20(1).
(2) A person shall not market follow-on formula which contravenes regulation 5, 7, 9, 10, 11, 12, 14(1), (2) or (3), 16, 18, 19 or 20(2).”.
(3) In regulation 20 (presentation (infant formula and follow-on formula))—
(a)for paragraph (1) substitute —
“(1) The presentation of an infant formula shall comply with the provisions of regulations 17(1)(e), (2), (3) and (4) and 19”; and
(b)for paragraph (2) substitute —
“(2) The presentation of a follow-on formula shall comply with the provisions of regulations 18(2) and 19.”.
(4) For regulation 26(1)(a) (export of infant formula to third countries) substitute—
“(a)regulation 5, 6, 8, 10, 11, 12, 14(1), (2) or (3), 17, 19 or 20(1);”.
(5) For regulation 27(a) (export of follow-on formula to third countries) substitute—
“(a)regulation 5, 7, 9, 10, 11, 12, 14(1), (2) or (3), 18, 19 or 20(2);”.
(6) For regulation 31(3) (revocation and transitional arrangements) substitute—
“(3) In respect of any contravention before 1st January 2010, a person does not commit an offence under regulation 28(1) consisting of a contravention of —
(a)regulation 3(1), where—
(i)the action that would otherwise constitute the offence consists of marketing infant formula which contravenes regulation 5, 6, 8, 10, 11, 12 or 14(1), (2) or (3), and
(ii)that action does not constitute an offence under regulation 10(1) of the 1995 Regulations consisting of a contravention of regulation 2(1)(a)(i) or (ii) of those Regulations;
(b)regulation 3(1), where—
(i)the action that would otherwise constitute the offence consists of marketing infant formula which contravenes regulation 17 or 19, and
(ii)that action, had it taken place on 10th January 2008, would not have constituted an offence under regulation 10(1) of the 1995 Regulations as they then stood consisting of a contravention of regulation 2(1)a (iii) of those Regulations;
(c)regulation 3(1), where—
(i)the action that would otherwise constitute the offence consists of marketing infant formula which contravenes regulation 20(1) in so far as regulation 20(1) applies in relation to the shape, appearance and packaging of that infant formula, and
(ii)that action, had it taken place on 10th January 2008, would not have constituted an offence under regulation 10(1) of the 1995 Regulations as they then stood consisting of a contravention of regulation 2(1)(a)(iv) of those Regulations in so far as regulation 2(1)(a)(iv) applied in relation to the shape, appearance and packaging of that infant formula;
(d)regulation 3(2), where—
(i)the action that would otherwise constitute the offence consists of marketing follow-on formula which contravenes regulation 5, 7, 9, 10, 11, 12 or 14(1), (2) or (3), and
(ii)that action does not constitute an offence under regulation 10(1) of the 1995 Regulations consisting of a contravention of regulation 2(2)(a) or (b) of those Regulations;
(e)regulation 3(2), where—
(i)the action that would otherwise constitute the offence consists of marketing follow-on formula which contravenes regulation 18 or 19, and
(ii)that action, had it taken place on 10th January 2008, would not have constituted an offence under regulation 10(1) of the 1995 Regulations as they then stood consisting of a contravention of regulation 2(2)(c) of those Regulations;
(f)regulation 3(2), where—
(i)the action that would otherwise constitute the offence consists of marketing follow-on formula which contravenes regulation 20(2) in so far as regulation 20(2) applies in relation to the shape, appearance and packaging of that follow-on formula, and
(ii)that action, had it taken place on 10th January 2008, would not have constituted an offence under regulation 10(1) of the 1995 Regulations as they then stood consisting of a contravention of regulation 2(2)(d) of those Regulations in so far as regulation 2(2)(d) applied in relation to the shape, appearance and packaging of that follow-on formula;
(g)regulation 4, where the action that would otherwise constitute the offence does not constitute an offence under regulation 10(1) of the 1995 Regulations consisting of a contravention of regulation 2(1)(b)(i) or (ii) of those Regulations;
(h)regulation 4, where the action that would otherwise constitute the offence, had it taken place on 10th January 2008, would not have constituted an offence under regulation 10(1) of the 1995 Regulations as they then stood consisting of a contravention of regulation 2(1)(b)(iii) of those Regulations; or
(i)regulation 4, where the action that would otherwise constitute the offence, had it taken place on 10th January 2008, would not have constituted an offence under regulation 10(1) of the 1995 Regulations as they then stood consisting of a contravention of regulation 2(1)(b)(iv) of those Regulations in so far as regulation 2(1)(b)(iv) applied in relation to the shape, appearance and packaging of the product concerned.”.
Annotations are used to give authority for changes and other effects on the legislation you are viewing and to convey editorial information. They appear at the foot of the relevant provision or under the associated heading. Annotations are categorised by annotation type, such as F-notes for textual amendments and I-notes for commencement information (a full list can be found in the Editorial Practice Guide). Each annotation is identified by a sequential reference number. For F-notes, M-notes and X-notes, the number also appears in bold superscript at the relevant location in the text. All annotations contain links to the affecting legislation.
Amendments (Textual)
F4S.R. 2007 No. 506
3.—(1) The Medical Food Regulations (Northern Ireland) 2000 F5 are amended in accordance with paragraph (2).
(2) The following regulation is inserted immediately after regulation 7 (application of various provisions of the Order)—
8. In respect of any contravention before 1st January 2010, a person does not commit an offence under regulation 5(a) consisting of a contravention of regulation 3(1)(a) where the action that would otherwise constitute the offence consists of selling a medical food whose composition fails to comply with Article 3 of the Directive as read with the row relating to manganese set out in the second part of Table I (minerals) in the Annex to the Directive if the composition of that medical food would have complied with Article 3 of the Directive as read with the row relating to manganese set out in the second part of Table I (minerals) in the Annex to the Directive as it stood before it was amended by Commission Directive 2006/141/EC on infant formulae and follow-on formulae and amending Directive 1999/21/EC.”.
Annotations are used to give authority for changes and other effects on the legislation you are viewing and to convey editorial information. They appear at the foot of the relevant provision or under the associated heading. Annotations are categorised by annotation type, such as F-notes for textual amendments and I-notes for commencement information (a full list can be found in the Editorial Practice Guide). Each annotation is identified by a sequential reference number. For F-notes, M-notes and X-notes, the number also appears in bold superscript at the relevant location in the text. All annotations contain links to the affecting legislation.
Amendments (Textual)
F5S.R. 2000 No. 187; the relevant amending instrument is S.R. 2007 No. 506
Sealed with the Official Seal of the Department of Health, Social Services and Public Safety on 2nd October 2008.
L.S.
Christine Jendoubi
A senior officer of the
Department of Health, Social Services and Public Safety
(This note is not part of the Regulations)
These Regulations amend the Infant Formula and Follow-on Formula Regulations (Northern Ireland) 2007 (S.R. 2007 No. 506) (“the 2007 Regulations”).
The amendments are required to give effect to the order of the High Court of Justice in Northern Ireland of 25th June 2008 in the matter of an application by the Infant and Dietetic Foods Association Ltd (“the IDFA”) for Judicial Review and in the matter of the Infant Formula and Follow-on Formula Regulations (NI) 2007 (case ref. CO1932838).
The order recited that the 2007 Regulations fail to comply with Commission Directive 2006/141/EC on infant formulae and follow-on formulae and amending Directive 1999/21/EC (OJ No. L401, 30.12.2006, p.1) to the extent that they prohibit as from 11 January 2008 (instead of as from 31 December 2009) trade in infant formula and follow-on formula whose labelling satisfies the labelling requirements of the Infant Formula and Follow-on Formula Regulations (Northern Ireland) 1995 (S.R. 1995 No. 85, as amended) but does not satisfy the labelling requirements of the 2007 Regulations.
These Regulations amend the Infant Formula and Follow-on Formula Regulations (Northern Ireland) 2007 to—
revise the list of regulations that must be complied with if a person is to market infant formula or follow-on formula (regulation 2(2));
provide that the presentation of infant formula and follow-on formula must comply with the provisions of specified regulations (regulation 2(3));
revise the list of regulations that must be complied with if a person is to export infant formula to third countries (regulation 2(4));
revise the list of regulations that must be complied with if a person is to export follow-on formula to third countries (regulation 2(5)); and
create transitional arrangements that apply in relation to the enforcement of—
the labelling requirements for infant formula and follow-on formula, (regulation 2(6) and
the requirements that apply in relation to the shape, appearance and packaging of infant formula and follow-on formula (regulation 2(6)). This amendment is considered necessary as a result of the judgments of the Court of Session in Scotland in the related case of the Petition of the IDFA and others for Judicial Review of a decision by the Scottish Ministers to make and lay before the Scottish Parliament the Infant Formula and the Follow-on Formula (Scotland) Regulations 2007 ([2008] CSOH87, case ref. P126/08)) and the High Court in England in the related case of R v the Secretary of State for Health and the Welsh Ministers on the application of the IDFA ( [2008] EWHC 575 (Admin), action number CO/230/2008.).
These Regulations also provide transitional arrangements with regard to the Medical Food Regulations (Northern Ireland) 2000 (S.R. 2000 No. 187) (regulation 3).
A full impact assessment has not been produced for this rule as no impact on the private or voluntary sectors is foreseen.
Latest Available (revised):The latest available updated version of the legislation incorporating changes made by subsequent legislation and applied by our editorial team. Changes we have not yet applied to the text, can be found in the ‘Changes to Legislation’ area.
Original (As Enacted or Made):The original version of the legislation as it stood when it was enacted or made. No changes have been applied to the text.
Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:
Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:
Click 'View More' or select 'More Resources' tab for additional information including: