There are currently no known outstanding effects for the The Genetically Modified Organisms (Deliberate Release) (Wales) Regulations 2002.
Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.
Part II DELIBERATE RELEASE OF ORGANISMS FOR ANY OTHER PURPOSE THAN FOR PLACING ON THE MARKET
Part III PLACING ON THE MARKET OF ORGANISMS AS OR IN PRODUCTS
Part IV DUTIES AFTER THE MAKING OF APPLICATIONS
20. Duty of the applicant after applying for consent to release or to market
21. Duties of the National Assembly for Wales on receiving applications for consent to release
22. Decisions by the National Assembly for Wales on applications for consent to release
23. Variation or revocation of a consent to release genetically modified organisms
24. Duties of the National Assembly for Wales in relation to applications for consent to market genetically modified organisms
25. Decisions by the National Assembly for Wales on applications for consent to market genetically modified organisms
26. Duties on the National Assembly for Wales on receiving applications for renewal of consent to market genetically modified organisms
27. Decisions by the National Assembly for Wales on applications for renewals of consents to market genetically modified organisms
28. Genetically modified organisms containing antibiotic resistance markers
Part II INFORMATION RELATING TO THE PARENTAL OR RECIPIENT PLANT
Part IV INFORMATION RELATING TO THE GENETICALLY MODIFIED PLANT
13.A description of the trait or traits and characteristics of...
14.The following information on the sequences actually inserted or deleted:...
15.The following information on the expression of the insert—
16.Information on how the genetically modified plant differs from the...
17.The genetic stability of the insert and phenotypic stability of...
18.Any change to the ability of the genetically modified plant...
19.Information on any toxic, allergenic or other harmful effects on...
20.Information on the safety of the genetically modified plant to...
21.The mechanism of interaction between the genetically modified plant and...
22.The potential changes in the interactions of the genetically modified...
24.A description of detection and identification techniques for the genetically...
25.Information about previous releases of the genetically modified plant, if...
Part V INFORMATION RELATING TO THE SITE OF RELEASE
Part VI INFORMATION RELATING TO THE RELEASE
(Applications for consent to release only)
30.The purpose of the release of the genetically modified plant,...
31.The foreseen date or dates and duration of the release....
32.The method by which the genetically modified plants will be...
33.The method for preparing and managing the release site, prior...
34.The approximate number of genetically modified plants (or plants per...
Part VII INFORMATION ON CONTROL, MONITORING, POST-RELEASE AND WASTE TREATMENT PLANS
Part II INFORMATION RELATING TO THE GENETICALLY MODIFIED ORGANISMS
Characteristics of donor, parental and recipient organisms
6.The degree of relatedness between donor and recipient or between...
7.The description of identification and detection techniques.
8.The sensitivity, reliability (in quantitative terms) and specificity of detection...
9.The description of the geographic distribution and of the natural...
10.The organisms with which transfer of genetic material is known...
11.Verification of the genetic stability of the organisms and factors...
12.The following pathological, ecological and physiological traits—
13.The sequence, frequency of mobilisation and specificity of indigenous vectors,...
Characteristics of the genetically modified organisms
25.The description of genetic trait or traits or phenotypic characteristics...
26.The structure and amount of any vector or donor nucleic...
27.The stability of the organisms in terms of genetic traits....
30.The description of identification and detection techniques, including techniques for...
31.The sensitivity, reliability (in quantitative terms), and specificity of detection...
32.The history of previous releases or uses of the organisms....
33.In relation to human health, animal health and plant health—...
Part III INFORMATION RELATING TO THE CONDITIONS OF RELEASE
34.The description of the proposed deliberate release, including the purpose...
35.The intended dates of the release and time planning of...
40.The disturbance of the site, including the type and method...
43.The techniques foreseen for elimination or inactivation of the genetically...
44.Information on, and the results of, previous releases of the...
The environment (both on the site and in the wider environment)
45.The geographical location and national grid reference of the site...
46.The physical or biological proximity of the site of the...
47.The proximity to significant biotopes, protected areas or drinking water...
48.The climatic characteristics of the region or regions likely to...
49.The geographical, geological and pedological characteristics.
50.The flora and fauna, including crops, livestock and migratory species....
51.The description of the target and non-target ecosystems likely to...
52.The comparison of the natural habitat of the recipient organisms...
53.Any known planned developments or changes in land use in...
Characteristics affecting survival, multiplication and dissemination
Interactions with the environment
57.The predicted habitat of the genetically modified organisms.
58.The studies on the behaviour and characteristics of the organisms...
59.The capability of post-release transfer of genetic material—
60.The likelihood of post-release selection leading to the expression of...
61.The measures employed to ensure and to verify genetic stability,...
62.The routes of biological dispersal, known or potential modes of...
63.The description of ecosystems to which the genetically modified organisms...
64.The potential for excessive population increase of the genetically modified...
65.The competitive advantage of the organisms in relation to the...
66.The identification and description of the target organisms if applicable....
67.The anticipated mechanism and result of interaction between the released...
68.The identification and description of non-target organisms which may be...
69.The likelihood of post release shifts in biological interactions or...
70.The known or predicted interactions with non-target organisms in the...
71.The known or predicted involvement of the organisms in biogeochemical...
72.Any other potential interactions of the organisms with the environment....
Part V INFORMATION ON MONITORING, CONTROL, WASTE TREATMENT AND EMERGENCY RESPONSE PLANS
83.Methods and procedures for controlling the genetically modified organisms in...
84.Methods, such as eradication of the genetically modified organisms, for...
85.Methods for disposal or sanitation of plants, animals, soils, and...
86.Methods for the isolation of the areas affected by the...
87.Plans for protecting human health and the environment in case...
INFORMATION TO BE INCLUDED IN AN APPLICATION FOR CONSENT TO MARKET GENETICALLY MODIFIED ORGANISMS
1.The proposed commercial name of the product and names of...
4.A description of how the product and the genetically modified...
5.A description of the geographical area or areas and types...
6.A description of the intended categories of users of the...
7.Information on the genetic modification for the purposes of placing...
8.The proposed labelling, which must include, in a label or...
Part II ADDITIONAL RELEVANT INFORMATION
10.Specific instructions or recommendations for storage and handling of the...
11.Specific instructions for carrying out monitoring and reporting to the...
12.The proposed restrictions in the approved use of the genetically...
14.The estimated product in and/or imports to the Community.
15.Any proposed additional labelling, which may include, at least in...
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. The revised version is currently only available in English.
Original (As Enacted or Made) - English: The original English language version of the legislation as it stood when it was enacted or made. No changes have been applied to the text.
Original (As Enacted or Made) - Welsh:The original Welsh language version of the legislation as it stood when it was enacted or made. No changes have been applied to the text.
Point in Time: This becomes available after navigating to view revised legislation as it stood at a certain point in time via Advanced Features > Show Timeline of Changes or via a point in time advanced search. A point in time version is only available in English.
Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:
This timeline shows the different points in time where a change occurred. The dates will coincide with the earliest date on which the change (e.g an insertion, a repeal or a substitution) that was applied came into force. The first date in the timeline will usually be the earliest date when the provision came into force. In some cases the first date is 01/02/1991 (or for Northern Ireland legislation 01/01/2006). This date is our basedate. No versions before this date are available. For further information see the Editorial Practice Guide and Glossary under Help.
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: