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The Genetically Modified Organisms (Deliberate Release and Risk Assessment) (Amendment) Regulations (Northern Ireland) 1997

S.R. 1997/534 · Made 11 December 1997 · Extends to Northern Ireland

Up to date with all changes known to legislation.gov.uk, revised to 15 April 2003.

EUROPEAN COMMUNITIES

ENVIRONMENTAL PROTECTION

Made 11th December 1997

Coming into operation 30th January 1998

The Department of the Environment, being a Department designatedf1 for the purposes of section 2(2) of the European Communities Act 1972f2, in relation to measures relating to the control and regulation of genetically modified organisms, in exercise of the powers conferred by that section and by Articles 5(7), 8(1), (4) and (7) of the Genetically Modified Organisms (Northern Ireland) Order 1991f3 and of all other powers enabling it in that behalf, hereby makes the following Regulations:

Annotations to the whole text

Footnotes

f1

S.I. 1991/755

f2

1972 c. 68

f3

S.I. 1991/1714 (N.I. 19). See Article 2(2) for the definition of “the Department”; see Articles 5(10) and 8(11) for the definition of “prescribed” in those Articles

Contents

  1. 1Citation, commencement and interpretation
  2. 2Amendment of the Genetically Modified Organisms (Deliberate Release) Regulations (Northern Ireland) 1994 Repealed
  3. 3Amendment of the Genetically Modified Organisms (Risk Assessment) (Records and Exemptions) Regulations (Northern Ireland) 1996
  4. Signature
  5. Schedule Schedule
  6. Explanatory note

1Citation, commencement and interpretationI1

(1)

These Regulations may be cited as the Genetically Modified Organisms (Deliberate Release and Risk Assessment) (Amendment) Regulations (Northern Ireland) 1997 and shall come into operation on 30th January 1998.

(2)

The Interpretation Act (Northern Ireland) 1954f1 shall apply to these Regulations as it applies to a Measure of the Northern Ireland Assembly.

2Amendment of the Genetically Modified Organisms (Deliberate Release) Regulations (Northern Ireland) 1994F1

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

3Amendment of the Genetically Modified Organisms (Risk Assessment) (Records and Exemptions) Regulations (Northern Ireland) 1996I1

In the Genetically Modified Organisms (Risk Assessment) (Records and Exemptions) Regulations (Northern Ireland) 1996f1 in paragraph (2) of regulation 4 (exemptions from requirement to carry out risk assessments) there shall be added at the end the following sub-paragraph—

“;

(e)

are or are contained in a novel food or novel food ingredient which is authorised for marketing in accordance with the provisions of Regulation (EC) No. 258/97 of the European Parliament and of the Council.”.

Signature

Sealed with the Official Seal of the Department of the Environment on

L.S.

R. W. Rogers

Assistant Secretary

11th December 1997.

I1

“SCHEDULE 2

INFORMATION TO BE CONTAINED IN AN APPLICATION FOR CONSENT TO MARKET GENETICALLY MODIFIED ORGANISMS

Regulation 11

Part I

General Information

1

The name of the product and the name of the genetically modified organisms in the product.

2

The name and address in the Community of the manufacturer or distributor of the product.

3

The specificity of the product and the exact conditions of use including, where appropriate, the type of environment and/or the geographical areas within the Community for which the product is suited.

4

The type of expected use of the product and the description of the persons who are expected to use the product.

4a

Information relating to the introduced genetic modification which could be of relevance to the establishment of a possible register of modifications introduced into organisms (species). This may include nucleotide sequences or any other type of information which is relevant for inclusion in such a register.

4b

Information regarding proposed labelling which must include, in a label or an accompanying document, an indication that the product contains, or consists of, genetically modified organisms. In the case of products to be placed on the market in mixtures with non-genetically modified organisms, it is sufficient to indicate the possibility that genetically modified organisms may be present.

Part II

Additional Relevant Information

5

The measures to be taken in the event of the escape of the organisms in the product or misuse of the product.

6

Specific instructions or recommendations for storage and handling of the product.

7

The estimated level and amount of production within the Community and the estimated level and amount of imports of the product into the Community.

8

Information regarding the proposed packaging for the product and its appropriateness so as to avoid the escape of genetically modified organisms during storage or at a later stage.

9

Information regarding proposed labelling including the proposals for stating, in full or summarised form, the information prescribed in paragraphs 1 to 3, 5 and 6.”

Explanatory note

(This note is not part of the Regulations.)

These Regulations implement as respects Northern Ireland Commission Directive 97/35/EC (O.J. No. L169, 27.6.97, p. 72) adapting to technical progress for the second time Council Directive 90/220/EEC on the deliberate release into the environment of genetically modified organisms, by amending the Genetically Modified Organisms (Deliberate Release) Regulations (Northern Ireland) 1994 (S.R. 1994 No. 144) (the 1994 Regulations).

Regulation 2(3) substitutes the Schedule for Schedule 2 to the 1994 Regulations.

In addition these Regulations amend the 1994 Regulations to take account of Regulation (EC) No. 258/97 (O.J. No. L43, 14.2.97, p. 1) concerning novel foods and novel food ingredients (the Novel Foods Regulation), with regard to the cases and circumstances in which a marketing consent is required under the 1994 Regulations.

These Regulations also amend the Genetically Modified Organisms (Risk Assessment) (Records and Exemptions) Regulations (Northern Ireland) 1996 (S.R. 1996 No. 442) to take account of the Novel Foods Regulation with regard to exemptions from the requirement to carry out risk assessments.

Copies of the Directive and Regulation and extracts from the Official Journal of the European Communities may be obtained from The Stationery Office, 16 Arthur Street, Belfast BT1 4GD.