2003 No. 579

PESTICIDES

The Plant Protection Products (Scotland) Regulations 2003
Made
26th November 2003
Laid before the Scottish Parliament
27th November 2003
Coming into force
31st December 2003
The Scottish Ministers, in exercise of the powers conferred by section 2(2) of the European Communities Act 1972 and of all other powers enabling them in that behalf, hereby make the following Regulations:

Citation, commencement and extent
1
1
These Regulations may be cited as the Plant Protection Products (Scotland) Regulations 2003 and shall come into force on 31st December 2003.
2
These Regulations extend to Scotland only.

Interpretation
2
1
In these Regulations–
- “the 1985 Act” means the Food and Environment Protection Act 1985 ;
- “active substance” means any substance or micro-organism, including a virus, having general or specific action against harmful organisms or on plants, parts of plants or plant products;
- “animals” means animals belonging to species normally fed and kept or consumed by humans;
- “approval” in relation to a plant protection product means an administrative act under these Regulations by which the Scottish Ministers, following an application submitted by an applicant, approve the placing on the market or use of that plant protection product in the whole or any part of Scotland and “approved” shall be construed accordingly;
- “the Commission” means the Commission of the European Communities;
- “contravenes” includes “fails to comply with”;
- “the Directive” means Council Directive 91/414/EEC concerning the placing of plant protection products on the market , as amended by the instruments listed in Schedule 1 to these Regulations;
- “the EEA” means the European Economic Area established under the EEA Agreement;
- “the EEA Agreement” means the Agreement on the EEA signed at Oporto on 2nd May 1992 as adjusted by the Protocol signed at Brussels on 17th March 1993 ;
- “EEA State” means a State which is a Contracting Party to the EEA Agreement;
- “the environment” means water, air, land, wild species of fauna and flora, and any interrelationship between them, as well as any relationship with living organisms;
- “equivalent provision” means any provision in any other Regulations made for the purposes of implementing the Directive, extending to any part of the United Kingdom, which has equivalent effect to a specified provision in these Regulations;
- “harmful organisms” means pests of plants or plant products belonging to the animal or plant kingdom, viruses, bacteria and mycoplasmas and other pathogens;
- “integrated control” means the rational application of a combination of biological, biotechnological, chemical, cultural or plant-breeding measures whereby the use of chemical plant protection products is limited to the minimum strictly necessary to maintain harmful organisms below levels above which economically unacceptable damage or loss would occur;
- “International Organisation for Standardisation” means the institution of that name founded in 1947 and currently having its headquarters at 1 Rue de Varembé, CP 56, 1211 Geneva 20, Switzerland;
- “International Union of Pure and Applied Chemistry” means the institution of that name founded in 1919 and currently having its headquarters at 104 T.W. Alexander Drive, Building 19, Research Triangle Park, NC 27709, USA;
- “new active substance” means any active substance which is not an old active substance;
- “old active substance” means any active substance which was on the market–
  1. in Austria, Finland, Iceland, Norway, Sweden and Liechtenstein, on or before 1st July 1994;
  2. in other States within the EEA, on or before 26th July 1993;
- “placing on the market” means any supply, whether in return for payment or not, within Scotland, including importation into Scotland from outside the EEA, other than a supply for storage followed by consignment from the EEA or disposal, and “place on the market” shall be construed accordingly;
- “plants” means live plants and live parts of plants including fresh fruit and seeds;
- “plant products” means products derived from plants in the unprocessed state or having undergone only simple preparation such as milling, drying or pressing, but excluding plants themselves;
- “plant protection product” means an active substance or a preparation containing one or more active substances, put up in the form in which it is supplied to the user, intended to–
  1. protect plants or plant products against all harmful organisms or prevent the action of such organisms;
  2. influence (for example, as a growth regulator) the life processes of plants, otherwise than as a nutrient;
  3. preserve plant products, in so far as such substances or products are not subject to provisions of Community law on preservatives;
  4. destroy undesired plants; or
  5. destroy parts of plants or check or prevent the undesired growth of plants;
- “preparation” means a mixture or solution composed of two or more substances, of which at least one is an active substance, and which is intended for use as a plant protection product;
- “the 1986 Regulations” means the Control of Pesticides Regulations 1986 ;
- “the relevant competent authorities” means the authorities appointed in the member States, other than the United Kingdom, for the purposes of carrying out the duties of a competent authority under the Directive;
- “residue” in relation to a plant protection product means one or more substances present in or on plants or products of plant origin, edible animal products or elsewhere in the environment and resulting from the use of that plant protection product, including its metabolites and products resulting from its degradation or reaction;
- “substance” means any chemical element and its compounds, as they occur naturally or by manufacture, and includes any impurity inevitably resulting from the manufacturing process;
- and other terms used in these Regulations have the same meaning as in the Directive.
2
A reference in these Regulations to anything done in writing or produced in written form includes a reference to an electronic communication, as defined in the Electronic Communications Act 2000 , which has been recorded and is consequently capable of being reproduced.
3
In these Regulations–
a
any reference to a numbered Article shall be construed as a reference to the Article so numbered in the Directive;
b
any reference to a numbered Annex shall be construed as a reference to the Annex so numbered of the Directive; and
c
any reference to a numbered regulation or Schedule shall be construed as a reference to the regulation or Schedule so numbered in these Regulations.

Prohibitions
3
1
No person shall place on the market any plant protection product unless–
a
it has been approved under regulation 5, 7, 8 or 11 or an equivalent provision; and
b
it is placed on the market in accordance with any requirement or condition which is specified in the approval.
2
No person shall use any plant protection product unless–
a
it has been approved under regulation 5, 7, 8 or 11 or an equivalent provision;
b
it is used in accordance with any requirement or condition which is–
i
specified in the approval or in any extension of use granted under regulation 10 or an equivalent provision; or
ii
required by the approval or extension of use to be on the labelling;
c
it is used in accordance with the principles of good plant protection practice; and
d
whenever possible, it is used in accordance with the principles of integrated control.
3
No person shall place on the market any new active substance unless–
a
that active substance is included in Annex I; or
b
an application (which has not yet been decided in accordance with the procedure in Article 19) has been made for the inclusion of that active substance in Annex I.
4
Paragraphs (1), (2) and (3) above shall not apply to any plant protection product or active substance which is approved under regulation 9 or an equivalent provision.
5
Nothing in this Regulation shall impede the production, storage or movement within Scotland of a plant protection product intended for use in an EEA State other than the United Kingdom, provided that–
a
the product is authorised by the competent authority of that EEA State for use in that EEA State; and
b
the inspection requirements laid down by that EEA State in order to ensure compliance with Article 3(1) are satisfied.
6
Any person who contravenes or causes or permits any person to contravene paragraph (1), (2)(a) or (b) or (3) above shall be guilty of an offence.

Applications concerning active substances
4
1
Any person who applies for the inclusion of a new active substance in Annex I shall submit to the Scottish Ministers, the relevant competent authorities and the Commission a dossier which satisfies the requirements of Annex II, a declaration that the active substance is intended for use in a plant protection product and a dossier complying with Annex III on at least one preparation containing that active substance.
2
Where any active substance has been included in Annex I, any person may make an application for variation of the conditions subject to which the active substance was included.
3
Any person who applies under paragraph (2) above shall submit the application to the Scottish Ministers, the relevant competent authorities and the Commission.
4
This regulation applies to any person whose principal place of business in Great Britain is situated in Scotland.

Standard approvals
5
1
Subject to the following provisions of this regulation and to regulation 6, the Scottish Ministers may approve, for a period not exceeding ten years, the placing on the market and use of any plant protection product.
2
The Scottish Ministers may renew an approval granted under this regulation after verification that the requirements of regulation 6(2) to (7) continue to be satisfied.
3
Where an application for renewal of an approval granted under this regulation has been made, the Scottish Ministers may renew the approval for a provisional period while they undertake the verification mentioned in paragraph (2) above.
4
Without prejudice to regulation 11, an applicant for approval of a plant protection product under this regulation shall submit with the application–
a
a dossier satisfying, in the light of current scientific and technical knowledge, the requirements set out in Annex III; and
b
for each active substance in the plant protection product, a dossier satisfying, in the light of current scientific and technical knowledge, the requirements set out in Annex II.
5
By way of derogation from paragraph (4) above, and without prejudice to the provisions of regulation 15(1) to (4), an applicant for approval of a plant protection product under this regulation shall be exempted from supplying the information required under paragraph (4)(b) above (except for that identifying the active substance) if the active substance is already included in Annex I at the time of the application, there being taken into account the conditions of inclusion in that Annex, and does not differ significantly in degree of purity and nature of impurities from the composition registered in the dossier accompanying the original application for inclusion of the active substance in Annex I.
6
An approval granted under this regulation shall specify the requirements and conditions relating to the placing on the market and use of the product and such requirements and conditions shall include all those necessary to comply with regulation 6(3)(a) to (e).
7
Any person who contravenes or causes or permits any person to contravene any requirement or condition of approval granted under this regulation shall be guilty of an offence.

General requirements for granting of standard approvals
6
1
The Scottish Ministers shall not approve a plant protection product under regulation 5 unless the requirements set out in paragraphs (2) to (7) below are satisfied in relation to it.
2
The active substances of the plant protection product shall have been included in Annex I at the time the approval is granted and any conditions laid down in that Annex shall have been fulfilled.
3
Having regard to current scientific and technical knowledge and upon the appraisal of the dossier submitted for the approval of the product, it shall have been established (pursuant to the uniform principles provided for in Annex VI) that, when used in accordance with regulation 3(2) and having regard to all normal conditions under which it may be used and the consequences of its use, the plant protection product–
a
is sufficiently effective;
b
has no unacceptable effects on plants or plant products;
c
does not cause unnecessary suffering and pain to vertebrates which are to be controlled;
d
has no harmful effect directly or indirectly on human or animal health (for example, through drinking water, food or feed) or on ground water;
e
has no unacceptable influence on the environment, having particular regard to–
i
its fate and distribution in the environment, particularly contamination of water (including drinking water and ground water); and
ii
its impact on non-target species; and
f
can be used in such a way that any provisional maximum residue levels determined by the Scottish Ministers under paragraph (7) below or by the Commission under Article 4(1)(f) are not exceeded.
4
The Scottish Ministers, pursuant to the uniform principles provided for in Annex VI, shall have determined the nature and quantity of the active substances of the plant protection product and, where appropriate, any toxicologically or ecotoxicologically significant impurities and co formulants, applying methods which, until harmonised methods have been adopted under Article 4(1)(c), they have determined are appropriate.
5
The Scottish Ministers, pursuant to the uniform principles provided for in Annex VI, shall have determined the residues of the plant protection product, resulting from approved uses, which are of toxicological or environmental significance, by applying appropriate methods in general use.
6
The Scottish Ministers, pursuant to the uniform principles provided for in Annex VI, shall have determined the physical and chemical properties of the plant protection product and shall have adjudged them to be acceptable for the purposes of the appropriate use and storage of the product.
7
The Scottish Ministers shall have determined provisional maximum residue levels for the agricultural products referred to in the approval and shall have notified them to the Commission.
8
The Scottish Ministers shall ensure that compliance with the requirements set out in paragraphs (2) to (7) above is achieved by official or officially recognised tests and analyses carried out under agricultural, plant health and environmental conditions relevant to the use of the plant protection product and representative of those prevailing where the product is intended to be used.

Provisional approvals
7
1
The Scottish Ministers may, to enable a gradual assessment to be made of the properties of new active substances and to make it easier for new preparations to be made available for use in agriculture, approve, for a provisional period not exceeding three years, the placing on the market and use of any plant protection product containing a new active substance which is not included in Annex I, provided that the conditions specified in paragraph (2) below are satisfied.
2
The conditions mentioned in paragraph (1) above are–
a
a dossier on the active substance has been submitted in accordance with regulation 4(1) and satisfies the requirements of Annexes II and III in relation to the projected uses;
b
the Scottish Ministers have established that the active substance can satisfy the requirements of Article 5(1) and that the plant protection product may be expected to satisfy the requirements of regulation 6(3) to (7).
3
When the conditions specified in paragraph (2) above have been satisfied the Scottish Ministers shall immediately inform the relevant competent authorities and the Commission of their assessment of the dossier and of the terms of the approval, giving at least the information provided for in Article 12(1).
4
If, following the examination provided for in Article 6(3) of a dossier submitted under regulation 4(1), it is decided, in accordance with the procedure laid down in Article 19, that the active substance does not satisfy the requirements specified in Article 5(1), the Scottish Ministers shall withdraw the provisional approval.
5
Before the expiry of an approval under paragraph (1) above and at the request of the approval holder, the Scottish Ministers may, subject to Article 8, extend that approval.
6
The Scottish Ministers shall ensure that compliance with the requirements set out in regulation 6(2) to (7) is achieved by official or officially recognised tests and analyses carried out under agricultural, plant health and environmental conditions relevant to the use of the plant protection product and representative of those prevailing where the product is intended to be used in Scotland.
7
An approval granted under this regulation shall specify the requirements and conditions relating to the placing on the market and use of the product and such requirements and conditions shall include at least all those necessary to comply with regulation 6(3)(a) to (e).
8
Any person who contravenes or causes or permits any person to contravene any requirement or condition of an approval granted under this regulation shall be guilty of an offence.

Emergency approvals
8
1
For the purposes of addressing a danger falling within Article 8(4), the Scottish Ministers may approve, for a period not exceeding 120 days, the placing on the market and use of any plant protection product not complying with regulation 6 for a limited and controlled use.
2
An approval granted under this regulation shall specify the requirements and conditions relating to the placing on the market and use of the product.
3
Any person who contravenes or causes or permits any person to contravene any requirement or condition of an approval granted under this regulation shall be guilty of an offence.

Approvals for research and development
9
1
No person shall carry out any experiment or test for research or development purposes involving the release into the environment of a plant protection product which has not been approved under regulation 5, 7, 8 or 11 unless an approval for trial purposes has been granted by the Scottish Ministers under this regulation in respect of that product.
2
Subject to paragraph (3) below, any person who wishes to obtain an approval under this regulation shall submit an application to the Scottish Ministers before the commencement of the experiment or test, together with a dossier containing all the available information, so as to permit an assessment to be made of possible effects on human or animal health or the possible impact on the environment.
3
Paragraph (2) above shall not apply if the Scottish Ministers have granted the applicant the right to undertake certain experiments and tests and have determined the conditions under which the experiments and tests have to be undertaken.
4
An approval granted under this regulation shall specify the requirements and conditions relating to the release into the environment of the product, which shall include a specification of the controlled conditions for carrying out the test, the quantities and area or location in respect of which the approval shall apply and any conditions imposed under paragraph (5) below.
5
If the proposed experiments or tests referred to in paragraph (1) above are liable to have harmful effects on human or animal health or to have an unacceptably adverse influence on the environment, the Scottish Ministers may either prohibit them or permit them subject to such conditions as they consider necessary to prevent those consequences.
6
This regulation shall not apply to experiments or tests covered by Part B of Council Directive 2001/18/EC on the deliberate release into the environment of genetically modified organisms .
7
Any person who contravenes or causes or permits any person to contravene–
a
paragraph (1) above; or
b
any requirement or condition of an approval granted under this regulation,
shall be guilty of an offence.

Extensions of approved use
10
1
Official or scientific bodies involved in agricultural activities or professional agricultural organisations and professional users may apply to the Scottish Ministers for the approved use of a plant protection product in Scotland to be extended to purposes other than those for which the approval of that product was granted.
2
The Scottish Ministers shall grant an extension of the approved use of a plant protection product when they consider that it is in the public interest and if–
a
the documentation and information to support the extension have been submitted by the applicant for extension;
b
the Scottish Ministers have established that the conditions referred to in regulation 6(3)(c),(d) and (e) are satisfied;
c
the intended use is minor in nature; and
d
users are fully and specifically informed as to instructions for use.
3
An extension of use granted under this regulation shall be for such a period, not exceeding the period for the approved use of the plant protection product, as may be specified in the extension and shall specify the requirements and conditions relating to the extended use of the product.
4
Any person who contravenes or causes or permits any person to contravene any requirement or condition of an extension of use granted under this regulation shall be guilty of an offence.

Mutual recognition of approvals
11
1
Where–
a
a plant protection product has been authorised under the Directive to be placed on the market and used in another EEA State; and
b
all the active substances contained in that plant protection product are included in Annex I,
any person may apply to the Scottish Ministers for approval of that plant protection product under this regulation.
2
An applicant for an approval under this regulation must substantiate the comparability requirement with documentary evidence.
3
To the extent that they are satisfied that the comparability requirement is met, the Scottish Ministers shall not require the repetition of tests and analyses already carried out in connection with the authorisation of the plant protection product in that other EEA State and shall grant the application.
4
An approval granted under this regulation may specify conditions resulting from the implementation of other measures in accordance with Community law, relating to the conditions for distribution and use of plant protection products intended to protect the health of the distributors, users and workers concerned.
5
An approval granted under this regulation may also specify conditions by way of restrictions on use which arise from differences in dietary patterns and are necessary in order to avoid exposure of consumers of treated products to the risks of dietary contamination in excess of the acceptable daily intake of the residues concerned.
6
An approval granted under this regulation may, with the agreement of the applicant, specify modifications in the requirements or conditions of use subject to which the plant protection product was authorised in order to render any non comparable agricultural, plant health or environmental (including climatic) conditions irrelevant for the purpose of satisfying the comparability requirement.
7
Any person who contravenes or causes or permits any person to contravene any requirement or condition of an approval granted under this regulation shall be guilty of an offence.
8
In this regulation “the comparability requirement” means the requirement that the agricultural, plant health and environmental (including climatic) conditions relevant to the use of the plant protection product in the EEA State in which it has been authorised to be placed on the market and used must be comparable to those in the United Kingdom.

Provisional restrictions and prohibitions
12
1
Where the Scottish Ministers reasonably consider that a product which they have approved, or are required to approve, under regulation 11 constitutes a risk to human or animal health or the environment, they may provisionally restrict or prohibit its sale or use in Scotland and shall immediately notify the holder of the approval or the applicant (as the case may be), the relevant competent authorities and the Commission of such action, giving reasons for the decision.
2
A provisional restriction or prohibition under paragraph (1) above shall survive so long as its survival is consistent with Article 11(2).

Applications, reviews, revocations and modifications
13
1
An application for approval of a plant protection product under regulation 5, 7, 8 or 11 shall be made to the Scottish Ministers by or on behalf of the person responsible for first placing it on the market in Scotland.
2
For the purpose of any application for an approval under these Regulations or for an extension of use under regulation 10–
a
the applicant shall have a permanent office within the EEA;
b
the applicant’s principal place of business in Great Britain shall be situated in Scotland;
c
the application shall be in English;
d
samples of the preparation and of its ingredients shall be provided if requested by the Scottish Ministers.
3
The Scottish Ministers may review an approval granted under regulation 5 or 7 or an extension of use granted under regulation 10, if there are indications that any of the relevant requirements are no longer satisfied.
4
When reviewing an approval or extension of use under paragraph (3) above the Scottish Ministers may require the holder of the approval or extension of use to submit further information necessary for the review, and the approval or extension of use may, where necessary, be extended for the period necessary to complete the review and provide such further information.
5
Without prejudice to any decision already taken pursuant to regulation 11, the Scottish Ministers, in relation to any approval granted under these Regulations or extension of use granted under regulation 10–
a
shall revoke the approval or extension of use if it is established that–
i
the requirements for obtaining the approval or extension of use are not or are no longer satisfied; or
ii
false or misleading particulars were supplied concerning the facts on the basis of which the approval or extension of use was granted;
b
may revoke the approval or extension of use if it is established that any requirement or condition which is–
i
specified in the approval or extension of use; or
ii
required by the approval or extension of use to be on the labelling,
is not or is no longer required;
c
may revoke the approval or extension of use at the request of the holder of the approval or the extension of use, who shall state the reasons for such a request.
6
Where the Scottish Ministers revoke an approval or extension of use under paragraph (5) above, they shall immediately inform the holder of the approval or extension of use of such revocation and may grant a period of grace for the disposal, storage, placing on the market and use of existing stocks, of a length commensurate with the reason for the revocation, without prejudice to any period provided for by a decision taken under Council Directive 79/117/EEC prohibiting the placing on the market and use of plant protection products containing certain active substances as amended or to Article 6(1) or 8(1) or (2).
7
Without prejudice to any decision already taken pursuant to regulation 11 and subject to paragraph (8) below, the Scottish Ministers, in relation to any approval granted under these Regulations or extension of use granted under regulation 10–
a
shall modify the approval or extension of use if it is established that on the basis of developments in scientific and technical knowledge the manner of use and amounts used can be modified;
b
may modify the approval or extension of use at the request of the holder of the approval or the extension of use, who shall state the reasons for such a request.
8
The Scottish Ministers may modify an approval or an extension of use under paragraph (7) above if it is established that the relevant requirements continue to be satisfied.
9
Before revoking an approval or extension of use under paragraph 5(a) or (b) above, or modifying an approval or extension of use under paragraph 7(a) above, the Scottish Ministers shall notify the holder of the approval or extension of use of their intention to revoke or modify the approval or extension of use (and of their grounds for doing so) and shall allow the holder such opportunity (if any) to make representations as the Scottish Ministers consider reasonable having regard to the reason why they think the revocation or modification is required.
10
Where, in the case of a revocation or modification referred to in paragraph (9) above, the Scottish Ministers do not allow any opportunity to make representations, they shall notify the holder in question as soon as is reasonably practicable of their grounds for not allowing it.
11
In this regulation “the relevant requirements” means–
a
in the case of an approval granted under regulation 5, the requirements of regulation 6(2) to (7);
b
in the case of an approval granted under regulation 7, the requirements of regulation 6(3) to (7);
c
in the case of an extension of use granted under regulation 10, the requirements of regulation 6(3)(c), (d) and (e).

Notification of information on potentially dangerous effects
14
1
The holder of any approval of a plant protection product granted under these Regulations, or the holder of any extension of use of a plant protection product granted under regulation 10, shall immediately notify the Scottish Ministers, the relevant competent authorities and the Commission of all new information on the potentially dangerous effects of that plant protection product, or of residues of an active substance contained in that plant protection product, on human or animal health, ground water or the environment.
2
Any person who contravenes or causes or permits any person to contravene paragraph (1) above shall be guilty of an offence.

Data protection
15
1
Subject to paragraph (2) below, the Scottish Ministers shall not make use of any information provided in accordance with Annex II by an applicant for approval of a plant protection product under regulation 5 or 7 for the benefit of any other applicant for approval of a plant protection product under regulation 5 or 7.
2
The Scottish Ministers may make use of such information in the circumstances provided for in Article 13(3).
3
Subject to paragraph (4) below, the Scottish Ministers shall not make use of any information provided in accordance with Annex III by an applicant for approval of a plant protection product under regulation 5 or 7 for the benefit of any other applicant for approval of a plant protection product under regulation 5 or 7.
4
The Scottish Ministers may make use of such information in the circumstances provided for in Article 13(4).
5
The Scottish Ministers, following examination of an application for approval of a plant protection product under regulation 5 or 7, shall inform the Commission of instances where they consider that an active substance as included in Annex I has been produced by a person or manufacturing process other than those specified in the dossier on the basis of which that active substance was first included in Annex I and shall transmit to the Commission all relevant information regarding the identity and impurities of that active substance.

Duplication of experiments
16
1
Notwithstanding regulation 5(4), and without prejudice to regulation 11, where an active substance has been included in Annex I–
a
any person who intends to apply for approval under regulation 5 or 7 of a plant protection product containing that substance, and who intends to use that plant protection product in an experiment involving vertebrate animals, shall enquire of the Scottish Ministers–
i
whether approval has already been granted for that plant protection product and, if so,
ii
as to the name and address of any holder of a previous or existing approval,
and shall supply evidence that they intend to apply for approval on their own behalf and that the other information specified in regulation 5(4) is available;
b
the Scottish Ministers, if satisfied that that person intends to make such an application, shall provide that person with the name and address of the holder or holders of previous or existing approvals and at the same time inform the holders of those approvals of the name and address of that person.
2
The holder or holders of previous approvals and the person intending to make the application shall take all reasonable steps to reach agreement on the sharing of information so as to avoid the duplication of testing on vertebrate animals.
3
Where a person requests any information with a view to inclusion of an old active substance in Annex I, the Scottish Ministers shall encourage holders of such information to co operate in the provision of the requested information, with a view to limiting the duplication of testing on vertebrate animals.
4
Where a person who intends to apply for approval of a plant protection product and holders of previous approvals of the same product cannot reach an agreement on the sharing of information, the Scottish Ministers may direct that person and holders of previous approvals located within Scotland to share the information with a view to avoiding duplicative testing on vertebrate animals and determine both the procedure for utilising information and the reasonable balance of the interests of the parties concerned.
5
Any person who–
a
fails to make enquiries as required in paragraph (1)(a) above; or
b
fails to comply with a direction made by the Scottish Ministers under paragraph (4) above,
shall be guilty of an offence.
6
Any person who causes or permits any person to–
a
fail to make enquiries as required in paragraph (1)(a) above; or
b
fail to comply with a direction made by the Scottish Ministers under paragraph (4) above,
shall be guilty of an offence.

Confidentiality
17
1
Subject to paragraphs (2) and (4) below, where an applicant for the inclusion of an active substance in Annex I or an applicant for approval of a plant protection product so requests, the Scottish Ministers shall treat any information submitted by that applicant as confidential to the extent that in the opinion of the Scottish Ministers that information contains industrial or commercial secrets.
2
The Scottish Ministers shall not treat as confidential the information specified in Schedule 2 and, once the application has been granted, the Scottish Ministers may make that information available to any person for inspection.
3
If subsequent to the request mentioned in paragraph (1) above the applicant discloses any information which is confidential by virtue of this regulation, the applicant shall inform the Scottish Ministers accordingly.
4
This regulation–
a
is without prejudice to the provisions of the Environmental Information Regulations 1992 , and
b
does not prohibit the provision, to any authority responsible for exercising any function under any equivalent provision, of information which the Scottish Ministers consider will assist the authority in exercising that function.

Packaging
18
1
No person shall place on the market a plant protection product unless the packaging of that product satisfies the following requirements:–
a
the packaging must be so designed and constructed that its contents cannot escape (unless special safety devices have been prescribed);
b
the materials constituting the packaging and fastenings must not be susceptible to attack by the contents, or liable to form harmful or dangerous compounds with the contents;
c
the packaging and fastenings must be strong and solid throughout so as to ensure that they will not come apart and will safely withstand normal handling; and
d
containers with fastening devices must be so designed that the container can be repeatedly refastened so that the contents cannot escape.
2
Any person who contravenes or causes or permits any person to contravene paragraph (1) above shall be guilty of an offence.

Labelling
19
1
No person shall place on the market a plant protection product unless–
a
the labelling of the packaging in which the product is contained satisfies the requirements specified in paragraphs 1 to 6 of Schedule 3; and
b
that person has complied with any requirement made by the Scottish Ministers under paragraph 7 of that Schedule.
2
Any person who contravenes or causes or permits any person to contravene paragraph (1) above shall be guilty of an offence.

Seizure and disposal of plant protection products
20
1
Where there has been a contravention, in relation to any plant protection product, of any prohibition, requirement or condition imposed by or under these Regulations or an equivalent provision in relation to that plant protection product, the Scottish Ministers shall have the power–
a
to seize or dispose of the plant protection product or require the holder of the approval, or any other person appearing to the Scottish Ministers to be the owner or the person in charge of that plant protection product, to dispose of it; or
b
to seize or dispose of anything treated with the plant protection product or require any person appearing to the Scottish Ministers to be the owner or the person in charge of anything so treated to dispose of it; or
c
to require the holder of the approval, or any other person appearing to the Scottish Ministers to be the owner or the person in charge of the plant protection product, to take such remedial action as appears to the Scottish Ministers to be necessary as a result of the contravention including, where it appears to be necessary as a result of the contravention, recovery of the plant protection product from the market in Scotland.
2
If any plant protection product has been imported into Scotland in contravention of these Regulations, the Scottish Ministers may, by notice in writing served on the person appearing to the Scottish Ministers to be the owner, the importer or the person in charge of the product, require that it shall be exported from Scotland within such period as the Scottish Ministers may reasonably determine.
3
Any person who contravenes or causes or permits any person to contravene any requirement imposed under this regulation shall be guilty of an offence.

General offences
21
1
Where in relation to an application for an approval under these Regulations, an application for an extension of use under regulation 10 or a requirement or condition specified in such an approval or extension of use, any person–
a
makes a statement which that person knows to be false in a material particular;
b
recklessly makes a statement which is false in a material particular; or
c
intentionally fails to disclose any material particular,
that person shall be guilty of an offence.
2
Where in relation to an application for an approval under these Regulations, an application for an extension of use under regulation 10 or a requirement or condition specified in such an approval or extension of use, any person causes or permits any person–
a
to make a statement which the former knows to be false in a material particular;
b
recklessly to make a statement which is false in a material particular; or
c
intentionally to fail to disclose any material particular,
that person shall be guilty of an offence.
3
Any person who–
a
intentionally obstructs an officer in the performance of any of the functions of that officer under regulation 24;
b
fails to comply with a requirement made or direction given by an officer in the performance of the functions of that officer under regulation 24; or
c
in purporting to give information required by an officer for the performance of any of the functions of that officer under regulation 24–
i
makes a statement which that person knows to be false in a material particular;
ii
recklessly makes a statement which is false in a material particular; or
iii
intentionally fails to disclose any material particular;
shall be guilty of an offence.
4
In this regulation “officer” shall have the same meaning as provided for in paragraph 1(c) of Schedule 2 to the 1985 Act, as read with regulation 24.

Penalties
22
1
A person guilty of an offence under regulation 3(6), 5(7), 7(8), 8(3), 9(7), 10(4), 11(7), 18(2), 19(2), 20(3) or 21(1) or (2) shall be liable–
a
on summary conviction, to a fine not exceeding the statutory maximum; and
b
on conviction on indictment, to a fine.
2
A person guilty of an offence under regulation 14(2), 16(5) or (6) or 21(3) shall be liable on summary conviction to a fine not exceeding level 5 on the standard scale.
3
Where an offence under these Regulations which has been committed by a body corporate is proved to have been committed with the consent or connivance of, or to be attributable to any neglect on the part of, a director, manager, secretary or other similar officer of the body corporate, or any person who was purporting to act in any such capacity, that person as well as the body corporate shall be guilty of that offence and be liable to be proceeded against and punished accordingly.
4
Where the affairs of a body corporate are managed by its members, paragraph (3) above shall apply in relation to the acts and defaults of a member in connection with the functions of management of that member as if that member were a director of the body corporate.
5
In paragraphs (3) and (4) above references to a “body corporate” include references to a Scottish partnership and, in relation to such partnership, any reference to a director or other officer of a body corporate is a reference to a partner.
6
Proceedings for any offence under these Regulations may be taken, and the offence may for the purposes of the jurisdiction of the court to try the offences be treated as having been committed, in any place in Scotland.
7
It shall be a defence in proceedings for an offence under section 7(b) of the Protection of Animals (Scotland) Act 1912 , which restricts the placing on land of poison and poisonous substances, for the person charged to show that they acted in accordance with an approval granted under these Regulations and, where appropriate, an extension of use granted under regulation 10.

General defence of due diligence
23
1
In any proceedings for an offence under these Regulations it shall be a defence for the person charged to prove that they took all reasonable precautions and exercised all due diligence to avoid the commission of the offence.
2
Without prejudice to the generality of paragraph (1) above, a person is to be taken to have established the defence provided by that paragraph if that person proves–
a
that they acted under instructions given by the employer of that person; or
b
that they acted in reliance on information supplied by another person without any reason to suppose that the information was false or misleading,
and in either case that they took all such steps as were reasonably open to them to ensure that no offence would be committed.
3
If in any case the defence provided by paragraph (1) above involves an allegation that the commission of the offence was due to an act or omission by another person, other than the giving of instructions to the person charged with the offence by the employer of that person, or to reliance on information supplied by another person, the person charged shall not, without leave of the court, be entitled to rely on that defence unless within a period ending seven clear days before the trial diet, that person has served on the prosecutor a notice giving such information identifying or assisting in the identification of that other person as was then in the possession of that person.

Enforcement
24
1
Section 19 of and paragraphs 1(c), 2 and 4 to 9 of Schedule 2 to the 1985 Act (enforcement powers) shall have effect for the purposes of these Regulations, as they have effect for the purpose of that Act and as if–
a
any reference in that section, or in those paragraphs, to that Act or a Part of it were a reference to these Regulations;
b
any reference in that section to a pesticide were a reference to a plant protection product; and
c
any reference in that section to an offence under section 16(12)(a) of that Act were a reference to an offence to which this regulation applies.
2
This regulation applies to any offence under regulation 3(6), 5(7), 7(8), 8(3), 9(7), 10(4), 11(7), 14(2), 16(5) or (6), 18(2), 19(2) or 20(3).

Service of documents
25
1
Any document required or authorised under these Regulations to be served by the Scottish Ministers on any person may be served–
a
by delivering it to that person or by leaving it at the proper address of that person or by sending it by post to that person at that address;
b
if the person is a body corporate, by serving it in accordance with sub-paragraph (a) above on the secretary of that body; or
c
if the person is a partnership, by serving it in accordance with sub-paragraph (a) above on a partner or a person having control or management of the partnership business.
2
For the purpose of this regulation and section 7 (which relates to the service of documents by post) of the Interpretation Act 1978 in its application to this regulation, the proper address of any person on whom a document is to be served shall be the last known address of that person, except that–
a
in the case of service on a body corporate or its secretary, it shall be the address of the registered or principal office of the body;
b
in the case of service on a partnership or a partner or a person having the control or management of a partnership business, it shall be the address of the principal office of the partnership,
and for the purpose of this paragraph the principal office of a company registered outside Scotland or of a partnership carrying on business outside Scotland includes its principal office within Scotland.
3
If a person to be served under these Regulations with any document has specified to the Scottish Ministers an address within Great Britain other than the proper address of that person (as determined under paragraph (2) above) as the one at which that person or someone on behalf of that person will accept documents of the same description as that document, that address shall also be treated as the proper address of that person for the purposes of this regulation and for the purposes of section 7 of the Interpretation Act 1978 in its application to this regulation.
4
In this regulation “secretary”, in relation to a local authority within the meaning of the Local Government (Scotland) Act 1973, means the proper officer within the meaning of that Act .

Agency arrangements
26
1
The Scottish Ministers may arrange, with the agreement of the UK Ministers, for any of their functions under or for the purposes of these Regulations or the Directive to be exercised on their behalf by a Minister of the Crown.
2
An arrangement under this regulation in respect of any function may include provisions for any fees and payments and levies payable under any enactment to any part of the Scottish Administration in respect of that function to be collected by a Minister of the Crown or Government Department on behalf of that part of the Scottish Administration.
3
An arrangement under this regulation shall be in writing and be signed by, or on behalf of, the Scottish Ministers and the UK Ministers and such an arrangement may be subject to such conditions (including conditions as to the costs and charge for costs) as may be agreed.

Transitional provisions
27
Schedule 4 shall have effect.

Disapplication
28
1
The 1986 Regulations shall not apply to any plant protection product the placing on the market and use of which are, or under Schedule 3 have become, subject to the prohibitions specified in regulation 3(1) and (2).
2
The 1986 Regulations shall not apply to any plant protection product which is approved under regulation 9.
3
The Farm and Garden Chemicals Regulations 1971 shall not apply to any plant protection product to the extent that regulation 19 applies to it.
4
In this regulation “pesticides”, “sale”, “supply” and “use” have the same meaning as in the 1986 Regulations.

Revocations
29
The Regulations specified in Schedule 5 are hereby revoked in relation to Scotland.
ROSS FINNIE
A member of the Scottish Executive
St Andrew’s House, Edinburgh
26th November 2003
SCHEDULE 1

INSTRUMENTS AMENDING COUNCIL DIRECTIVE 91/414/EEC
Regulation 2
Instruments | Active substances added to annex i
Commission Directive 93/71/EEC ; | None
Commission Directive 94/37/EC ; | None
Commission Directive 94/79/EC ; | None
Commission Directive 95/35/EC ; | None
Commission Directive 95/36/EC ; | None
Commission Directive 96/12/EC ; | None
Commission Directive 96/46/EC ; | None
Commission Directive 96/68/EC ; | None
Council Directive 97/57/EC ; | None
Commission Directive 2000/80/EC ; | lambda-cyhalothrin, imazalil, azoxystrobin, kresoxim-methyl, spiroxamine, azimsulfuron, fluroxypyr, metsulfuron-methyl, triasulfuron, esfenvalerate, prohexadione-calcium and bentazone
Commission Directive 2001/21/EC ; | amitrole, diquat, pyridate and thiabendazole
Commission Directive 2001/28/EC ; | Fenhexamid
Commission Directive 2001/36/EC ; | None
Commission Directive 2001/47/EC ; | Paecilomyces fumosoroseus
Commission Directive 2001/49/EC ; | flupyrsulfuron-methyl
Commission Directive 2001/87/EC ; | acibenzolar-s-methyl, cyclanilide, ferric phosphate, pymetrozine and pyraflufen-ethyl
Commission Directive 2001/99/EC ; | glyphosate and thifensulfuron-methyl
Commission Directive 2001/103/EC ; | 2,4-dichlorophenoxy acetic acid
Commission Directive 2002/18/EC ; | Isoproturon
Commission Directive 2002/37/EC | ethofumesate
Commission Directive 2002/48/EC ; | Iprovalicarb, prosulfuron and sulfosulfuron
Commission Directive 2002/64/EC ; | cinidon-ethyl, cyhalofop-butyl, famoxadone, florasulam, metalaxyl-M and picolinafen
Commission Directive 2002/81/EC ; | flumioxazine
Commission Directive 2003/5/EC ; | deltamethrin
Commission Directive 2003/23/EC ; | imazamox, oxasulfuron, ethoxysulfuron, foramsulfuron, oxadiargyl, cyazofamid
Commission Directive 2003/68/EC ; | trifloxstrobin, carfentrazone-ethyl, mesotrione, fenamidone, isoxaflutole
Commission Directive 2003/82/EC ; | None
As from 1st January 2004 amended by: Commission Directive 2003/31/EC ; | 2,4-DB, maleic hydrazide, cyfluthrin, beta-cyfluthrin, iprodione, linuron, pendimethalin
Commission Directive 2003/79/EC | coniothyrium minitans
Commission Directive 2003/84/EC | flurtamone, flufenacet, iodosulfuron, dimethenamid p, picoxystrobin, fosthiazate, silthiofam
As from 1st April 2004 amended by: Commission Directive 2003/39/EC | propyzamide, propineb
As from 1st June 2004 amended by: Commission Directive 2003/70/EC | mecoprop, mecoprop P, propiconazole
As from 1st August 2004 amended by: Commission Directive 2003/81/EC | molinate, thiram, ziram
SCHEDULE 2

NON-CONFIDENTIAL INFORMATION
Regulation 17
1
The name and content of the active substance and the name of the plant protection product.
2
The name of other substances which are regarded as dangerous under–
a
Council Directive 67/548/EEC on the approximation of laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances as amended ; and
b
Council Directive 1999/45/EC concerning the approximation of the laws, regulations and administrative provisions of the Member States relating to the classification, packaging and labelling of dangerous preparations as amended .
3
Physico-chemical data concerning the active substance and plant protection product.
4
Any ways of rendering the active substance or plant protection product harmless.
5
A summary of the results of the tests to establish the efficacy and harmlessness to humans, animals, plants and the environment of the active substance or the plant protection product.
6
Recommended methods and precautions to reduce handling, storage, transport, fire or other hazards.
7
The methods of analysis referred to in regulation 6(4) and (5) and Article 5.1.
8
Methods of disposal of the product and of its packaging.
9
Decontamination procedures to be followed in the case of accidental spillage or leakage.
10
First aid and medical treatment to be given in the case of injury to persons.
SCHEDULE 3

LABELLING
Regulation 19
1
The packaging containing the plant protection product shall be marked clearly and indelibly with the following information–
a
the trade name or designation of the plant protection product;
b
the name and address of the holder of the approval and the approval number of the plant protection product and, if different, the name and address of the person responsible for the final packaging and labelling or for the final labelling of the plant protection product on the market;
c
the name and the amount of each active substance; the name must be–
i
the same as that listed in Annex I to the Council Directive 67/548/EEC, if any;
ii
the common name given by the International Organization for Standardization, if any; or
iii
its chemical designation according to the rules of the International Union of Pure and Applied Chemistry contained in the Nomenclature of Organic Chemistry, 1979 edition as read with A Guide to IUPAC Nomenclature of Organic Components (recommendations 1993) ;
d
the net quantity of plant protection product given in legal units of measurements;
e
the formulation batch number or some means of identifying it;
f
the particulars required for the product in Articles 10 to 12 of Council Directive 1999/45/EC;
g
the nature of any special risks for humans, animals or the environment, by means of standard phrases selected as appropriate from those given in Annex IV;
h
safety precautions for the protection of humans, animals or the environment, in the form of standard phrases selected as appropriate from those given in Annex V;
i
the type of action of the plant protection product;
j
the type of preparation;
k
the uses for which the plant protection product has been approved and any specific agricultural, plant health and environmental conditions under which the product may be used or should not be used;
l
directions for use and the dose rate, expressed in metric units, for each use provided for under the terms of the approval;
m
where necessary, the safety interval for each use between application and–
i
sowing or planting of the crop to be protected;
ii
sowing or planting of succeeding crops;
iii
access by humans or animals;
iv
harvesting; and
v
use or consumption;
n
particulars of possible phytotoxicity, varietal susceptibility and any other direct or indirect adverse side effects on plants or products of plant origin together with the intervals to be observed between application and sowing or planting of–
i
the crop in question; or
ii
subsequent crops;
o
if accompanied by a leaflet, as provided for in paragraph 2 below, the sentence “Read accompanying instructions before use”;
p
directions for safe disposal of the plant protection product and of the packaging;
q
the expiry date relevant to normal conditions of storage where the shelf life of the product is limited to less than two years;
r
whether or not the product is restricted to a certain category of user.
2
The requirements specified in paragraphs (1), (m) and (n) of paragraph 1 above may be indicated on a separate leaflet accompanying the package if the space available on the package is too small and in such a case the leaflet shall be regarded as part of the label for the purposes of these Regulations.
3
In no circumstances may the label of the packaging of a plant protection product bear the indications “non-toxic”, “harmless” or similar indications.
4
Information to the effect that the plant protection product may be used when bees or other non-target species are active, or when crops or weeds are in flower, or other such phrases to protect bees or other non-target species, may be given on the label if the approval relates explicitly to use during the season for bees or other specified organisms and presents minimal risk to them.
5
Labels shall be in English.
6
At any time the Scottish Ministers may require additional phrases to be clearly and indelibly marked on packaging where this is deemed by them to be necessary for the protection of human beings, animals or the environment and where they make such a requirement they shall do so in writing by notice served on persons holding approvals for the plant protection products concerned.
7
The Scottish Ministers may require any of the persons referred to in paragraph 1(b) above at any time to provide them with samples, models or drafts of the packaging, labelling and leaflets referred to in this Schedule.
SCHEDULE 4

TRANSITIONAL PROVISIONS
Regulation 27

Application of these Regulations and of the 1986 Regulations to relevant plant protection products
1
Notwithstanding regulation 3(1) and (2) and subject to the remaining provisions of this Schedule–
a
these Regulations shall not apply; and
b
the 1986 Regulations shall continue to apply,
to a relevant plant protection product.
2
Notwithstanding paragraph 1 above, and subject to paragraphs 3 and 4 below, regulations 1, 2 and 9 and (insofar as they relate to approvals granted under regulation 9) regulations 13(2) and (5) to (8), 14, 17 and 20 to 28 shall apply to a relevant plant protection product.
3
Regulation 9 shall not apply to a relevant plant protection product to which any of the exemptions provided in regulation 3(2)(a) to (c) and (e) to (j) of the 1986 Regulations applies.
4
Notwithstanding regulation 28(2), a pesticide approval in respect of a relevant plant protection product given in the form of an experimental permit under regulation 5(a) of the 1986 Regulations which was in force on 13th November 1997 shall continue to be subject to the 1986 Regulations and shall continue in force until the date of expiry of such approval or earlier revocation under those Regulations.

Effect of Annex I decisions on the placing on the market and use of relevant plant protection products which are not approved pesticides
5
Where in relation to a relevant plant protection product which is not an approved pesticide it is decided under Article 6–
a
that the relevant active substances of that product should be included in Annex I, or
b
that any of the relevant active substances of that product should not be included in Annex I,
the placing on the market and use of that product shall become subject to the prohibitions specified in regulation 3(1) and (2).

Effect of a refusal to include an active substance in Annex I on relevant plant protection products which are approved pesticides
6
Where, in relation to a relevant plant protection product which is an approved pesticide, it has been decided under Article 6 that any of its relevant active substances should not be included in Annex I, the Scottish Ministers shall notify the pesticide approval holder of that decision and shall take the action described in paragraph 9(1) below.

Effect of a decision to include active substances in Annex I on relevant plant protection products which are approved pesticides
7
1
Where, in relation to any relevant plant protection product which is an approved pesticide, it has been decided under Article 6 that its relevant active substances should be included in Annex I, the Scottish Ministers shall notify the pesticide approval holder of that fact and the pesticide approval holder shall, within such period as the Scottish Ministers may determine and notify to the pesticide approval holder, provide information to the Scottish Ministers to show:
a
that the relevant active substances contained in the plant protection product comply with the conditions of Annex I inclusion; and
b
that the pesticide approval holder has access to a dossier satisfying the requirements of Annex II.
2
After having submitted to the Scottish Ministers the information required under paragraph (1) above, the pesticide approval holder may continue to place on the market and use the relevant plant protection product until such time as the Scottish Ministers notify the pesticide approval holder of their decision that they are or are not satisfied that the information provided shows that the relevant active substances comply with the conditions of Annex I inclusion and that the pesticide approval holder has access to a dossier satisfying the requirements of Annex II.
3
Where the pesticide approval holder fails to provide adequate information to enable the Scottish Ministers to reach a decision, the Scottish Ministers shall notify the pesticide approval holder of that failure and the pesticide approval holder shall, within such reasonable period as may be specified in the notification, submit further information to the Scottish Ministers to enable them to reach a decision.
4
Where the Scottish Ministers decide that the information provided under paragraph (1) above fails to show that the relevant active substances comply with the conditions of Annex I inclusion and that the pesticide approval holder has access to a dossier satisfying the requirements of Annex II they shall take the action described in paragraph 9(1) below.
8
1
Where the Scottish Ministers have determined that the information provided by the pesticide approval holder under paragraph 7 above shows that the relevant active substances comply with the conditions of Annex I inclusion and that the pesticide approval holder has access to a dossier satisfying the requirements of Annex II they shall notify the pesticide approval holder of that fact and the pesticide approval holder shall, within such period as the Scottish Ministers may determine and notify to the pesticide approval holder, make an application for an approval of the relevant plant protection product under regulation 5.
2
The pesticide approval holder may continue to place on the market and use the relevant plant protection product until such time as the Scottish Ministers notify the pesticide approval holder of their decision to grant or refuse an approval under regulation 5.
3
Where the pesticide approval holder fails to provide adequate information to enable the Scottish Ministers to consider the application, the Scottish Ministers shall notify the pesticide approval holder of that failure and the pesticide approval holder shall, within such reasonable period as may be specified in the notification, submit further information to the Scottish Ministers to enable them to consider the application.

Revocation of pesticide approval
9
1
The Scottish Ministers shall, at the same time as they notify a pesticide approval holder of a decision mentioned in paragraph 6, 7(4) or 8(2) above, revoke the pesticide approval.
2
The Scottish Ministers may, if any pesticide approval holder fails to comply with a notification given under paragraph 7(1) or (3) or 8(1) or (3) above, revoke the pesticide approval.
3
Where the Scottish Ministers revoke a pesticide approval under sub paragraph (1) or (2) above, they may revoke that approval–
a
completely;
b
in the manner specified in sub-paragraph (4) below; or
c
in the manner specified in sub-paragraph (5) below.
4
When revoking an approval in the manner mentioned in paragraph (b) of sub paragraph (3) above, the Scottish Ministers shall–
a
subject to sub paragraph (b) below, revoke that approval in so far as it authorises the advertisement, sale, storage, supply and use of that product; and
b
in the form of a provisional approval granted under regulation 5 of the 1986 Regulations for a period not exceeding one year commencing with the date of that revocation, authorise–
i
the storage of that product by any person; and
ii
the advertisement, sale, supply and use of that product by any person other than the pesticide approval holder or the pesticide approval holder’s employees or agents.
5
When revoking an approval in the manner mentioned in paragraph (c) of sub paragraph (3) above, the Scottish Ministers shall–
a
subject to sub paragraphs (b) and (c) below, revoke that approval in so far as it authorises the advertisement, sale, supply, storage and use of that product;
b
in the form of a provisional approval granted under regulation 5 of the 1986 Regulations for a period not exceeding one year commencing with the date of that revocation, authorise the advertisement, sale, storage, supply and use of that product by any person; and
c
in the form of a provisional approval granted under regulation 5 of the 1986 Regulations for a period, not exceeding one year following the end of the period of provisional approval granted under sub paragraph (b) above, authorise–
i
the storage of that product by any person; and
ii
the advertisement, sale, supply and use of that product by any person other than the pesticide approval holder or the pesticide approval holder’s employees or agents.

Effect of revocation on the placing on the market and use of the product
10
1
Where the Scottish Ministers have revoked a pesticide approval in relation to any plant protection product under paragraph 9(1) or (2) above completely, the placing on the market and use of that product shall become subject to the prohibitions specified in regulation 3(1) and (2) forthwith.
2
Where the Scottish Ministers have revoked a pesticide approval in relation to any plant protection product in the manner specified in paragraph 9(4) above, the placing on the market and use of that product shall become subject to the prohibitions specified in regulation 3(1) and (2) on the expiry of the period of the provisional approval granted under paragraph 9(4)(b) above.
3
Where the Scottish Ministers have revoked a pesticide approval in relation to any plant protection product in the manner specified in paragraph 9(5) above, the placing on the market and use of that product shall become subject to the prohibitions specified in regulation 3(1) and (2) on the expiry of the period of the provisional approval granted under paragraph 9(5)(c) above.

Notifications
11
Any notification given by the Scottish Ministers under this Schedule shall be in writing.

Interpretation
12
For the purposes of this Schedule–
- “approved pesticide” means a pesticide which is the subject of a pesticide approval;
- “pesticide approval” means approval of a pesticide given under regulation 5 of the 1986 Regulations;
- “pesticide approval holder” means any person who holds a current pesticide approval;
- “relevant active substance” means an active substance contained in a relevant plant protection product which is an approved pesticide;
- “relevant plant protection product” means any plant protection product–
  1. which is a pesticide, or substance, preparation or organism prepared or used for any of the purposes mentioned in regulation 3(1)(b) of the 1986 Regulations; and
  2. at least one of whose active ingredients is an old active substance; and
- “active ingredient”, “advertisement”, “organism”, “pesticide”, “preparation”, “sale”, “storage”, “substance”, “supply” and “use” have the same meanings as in the 1986 Regulations.
SCHEDULE 5

REVOCATIONS
Regulation 29
The following Regulations are hereby revoked–
The Plant Protection Products Regulations 1995 | S.I. 1995/887
The Plant Protection Products (Amendment) Regulations 1997 | S.I. 1997/7
The Plant Protection Products (Amendment) (No. 2) Regulations 1997 | S.I. 1997/2499
The Plant Protection Products Amendment (Scotland) Regulations 2001 | S.S.I. 2001/161
The Plant Protection Products Amendment (No. 3) (Scotland) Regulations 2001 | S.S.I. 2001/454
The Plant Protection Products Amendment (Scotland) Regulations 2002 | S.S.I. 2002/117
The Plant Protection Products Amendment (No. 2) (Scotland) Regulations 2002 | S.S.I. 2002/279
The Plant Protection Products Amendment (No. 3) (Scotland) Regulations 2002 | S.S.I. 2002/537
(This note is not part of the Regulations)
These Regulations revoke and replace the Plant Protection Products Regulations 1995 (S.I. 1995/887) insofar as they extend to Scotland.
The Regulations, which consolidate the 1995 Regulations (as amended) with modifications, continue to implement in Scotland Council Directive 91/414/EEC (O.J. No. L 230, 19.8.91, p.1 to be read with corrigenda published in O.J. No. L 170, 25.6.92, p.40) concerning the placing of plant protection products on the market (“the 1991 Directive”). The Regulations continue to implement the Directives amending the 1991 Directive, up to and including Commission Directive 2002/81/EC and also implement Commission Directives 2003/5/EC, 2003/23/EC, 2003/68/EC, 2003/31/EC, 2003/79/EC, 2003/84/EC, 2003/39/EC, 2003/70/EC, 2003/81/EC and 2003/82/EC which amend the 1991 Directive and which were not covered by the 1995 Regulations – see Schedule 1.
The 1991 Directive and Directive 93/71/EEC were extended to the European Economic Area (“the EEA”) by Decision No. 7/94 of the EEA Joint Committee (O.J. No. L 160, 28.6.94, p.1), which amended the European Economic Area Agreement (see Decision 94/1 ECSC, EEC; O.J. No. L 1, 3.1.94, p.1).
The Directive (as extended to the EEA) establishes an authorisation system whereby plant protection products (defined in the Directive as active substances and preparations containing one or more active substances intended inter alia to protect plants against harmful organisms) may not be placed on the market and used in the territory of an EEA State unless they have been authorised under the Directive by that EEA State (or, subject to qualifications, by another EEA State), The Directive (as read with adaptations set out in Decision No. 7/94 of the EEA Joint Committee) establishes uniform rules on the conditions and procedures for authorisation, including rules on the mutual recognition of authorisations between EEA States. The purpose of the system is to ensure that wherever they are placed on the market and used within the EEA plant protection products are effective without causing harm to human or animal health and without adversely affecting plants and ground water or the environment in general.
Before a plant protection product can receive a standard authorisation all its active substances must be included in Annex I to the Directive although the Directive allows provisional authorisation of a product in advance of such inclusion.
The inclusion of active substances which were on the market of EEA States on or before 26th July 1993 (or, as far as Austria, Finland, Iceland, Liechtenstein, Norway and Sweden are concerned, on or before 1st July 1994) are subject to a rolling review programme operated by the European Commission in conjunction with the member States of the European Community, although in transitional provisions set out in the Directive EEA States are permitted to authorise the placing on the market of products containing such substances until they have been reviewed; whereas inclusion of a new active substance in Annex I requires an application by the person intending to place it on the market.
The Directive also permits authorisations for short periods in the event of emergency and authorisations for releasing plant protection products into the environment for trial purposes. Authorisations are for fixed periods and in the case of standard authorisations they may be renewed on expiry. They may also be modified, or their range of application may be extended, in certain circumstances. Authorisations are subject to special requirements and conditions determined by the EEA State granting the authorisation, the breach of which would occasion automatic revocation. Authorisations carry a general requirement to notify the authorising EEA State of new information on the potentially dangerous effects of the authorised plant protection product or of residues of its active substances.
The Directive additionally provides certain data protection and confidentiality safeguards for holders of authorisations (whilst providing in certain circumstances for the release of information to other applicants and for the inspection of information by the public) and makes provision for the sharing of information between applicants and holders of previous authorisations of the same plant protection products with a view to limiting the duplication of tests on vertebrate animals. In addition, it prescribes requirements for labelling and packaging with which plant protection products must comply if they are to be placed on the market in the territory of an EEA State.
The Regulations continue to implement the provisions of the Directive described above by providing for the authorisation system in Scotland under the operation of the Scottish Ministers. In the Regulations authorisations are described as approvals. The Regulations impose a prohibition on the placing on the market and use of plant protection products unless they have been approved by the Scottish Ministers under the Regulations and are placed on the market and used in accordance with any conditions or requirements specified in their approval (regulation 3(1) and (2)). Persons intending to place new active substances on the market must apply to the Scottish Ministers for such substances to be included in Annex I (regulations 3(3) and 4(1)).
Applications for standard, provisional and emergency approvals of plant protection products and applications for approval of plant protection products already authorised under the Directive for use in another EEA State are made to the Scottish Ministers by the persons responsible for first placing the products on the market in Scotland (regulations 5 to 8, 11 and 13). Similarly, applications for approvals for trial purposes are made to the Scottish Ministers (regulation 9). The provisions of the Directive concerning extensions of the range of application of approved plant protection products and the provisions requiring the notification of potentially dangerous effects of approved plant protection products are respectively incorporated in regulations 10 and 14.
The data protection, information-sharing and confidentiality provisions of the Directive are set out in regulations 15, 16 and 17 and Schedule 2 and the provisions concerning the labelling and packaging of plant protection products are set out in regulations 18 and 19 and Schedule 3.
The Regulations confer enforcement powers on officers (who for specified purposes may be officers of local authorities) authorised by Scottish Ministers, including powers to seize and dispose of plant protection products in the event of a breach of a prohibition, requirement or condition imposed by or under the Regulations, to enter on land and to effect certain other controls (regulations 20 and 24). The Regulations make such breaches a criminal offence (see regulations 3, 5, 7, 8, 9, 10, 11, 14, 16, 18 and 19), create certain other types of offence (regulation 21) and prescribe penalties and defences (regulations 22 and 23).
The Regulations make provision to allow the Scottish Ministers to arrange with a Minister of the Crown for the discharge of any functions of the Scottish Ministers under the Regulations to be exercised on their behalf by a Minister of the Crown. Such an arrangement may include provision for any fees payable under any enactment to any part of the Scottish Administration in respect of that function to be collected by a Minister of the Crown or Government Department on behalf of that part of the Scottish Administration (regulation 26).
The transitional and consequential provisions (including those specifying the extent to which the Control of Pesticides Regulations 1986 (S.I. 1986/1510) will continue to apply) are contained in regulations 27 and 28 and Schedule 4.
Instruments which are revoked in relation to Scotland are set out in Schedule 5 (regulation 29).
A compliance cost assessment has not been prepared in respect of these Regulations.
A list of competent authorities of the member States of the European Community, to whom certain information and documents are required under the Regulations to be forwarded, can be obtained from the Pesticides Safety Directorate, Room 308, Mallard House, Kings Pool, 3 Peasholme Green, York YO1 2PX or via the website www.pesticides.gov.uk.
1972 c. 68. Section 2(2) was amended by the Scotland Act 1998 (c. 46), Schedule 8, paragraph 15(3). The functions conferred upon the Minister of the Crown under section 2(2) of the European Communities Act 1972, in so far as within devolved competence, were transferred to the Scottish Ministers by virtue of section 53 of the Scotland Act 1998.
1985 c. 48; section 19 was amended by the Pesticides (Fees and Enforcement) Act 1989 (c. 27), section 2, and by the Pesticides Act 1998 (c. 26), section 2.
O.J. No. L 230, 19.8.91, p.1 as read with the Corrigenda published in O.J. No. L 170, 25.6.92, p.40.
The EEA Agreement came into force on 1st January 1994 (see Decision 94/1 ECSC, EEC; O.J. No. L 1, 3.1.94, p.1). Protocol 47 and certain Annexes to the EEA Agreement were amended by Decision No. 7/94 of the EEA Joint Committee which came into force on 1st July 1994 (O.J. No. L 160, 28.6.94, p.1) Council Directive 91/414/EEC and Commission Directive 93/71/EEC (whose entry into force predated the entry into force of the EEA Agreement) were added to Chapter XV of Annex II to the EEA Agreement by item J in Annex 3 to that Decision (p.44), thus extending these Directives to the EEA.
S.I. 1986/1510, amended by S.I. 1997/188 and 2001/880.
2000 (c. 7).
O.J. No L 106, 17.4.01, p.1.
O.J. No. L 33, 8.2.79, p.36.
Last amended by Council Regulation 807/2003/EC (O.J. No. L 122, 16.5.03, p.36).
S.I. 1992/3240 amended by 1998/1447.
1912 c. 14.
1978 c. 30.
1973 c. 65.
S.I. 1971/1729.
O.J. No. L 221, 31.8.93, p.27, (as read with corrigenda published in O.J. No. L 170, 25.6.92, p.40).
O.J. No. L 194, 29.7.94, p.65.
O.J. No. L 354, 31.12.94, p.16, (as read with corrigenda published in O.J. No. L 280, 23.11.95, p.58).
O.J. No. L 172, 22.7.95, p.6.
O.J. No. L 172, 22.7.95, p.8.
O.J. No. L 65, 15.3.96, p.20.
O.J. No. L 214, 23.8.96, p.18.
O.J. No. L 277, 30.10.96, p.25.
O.J. No. L 265, 27.9.97, p.87.
O.J. No. L 309, 9.12.00, p.14.
O.J. No. L 69, 10.3.01, p.17.
O.J. No. L 113, 24.4.01, p.5.
O.J. No. L 164, 20.6.01, p.1.
O.J. No. L 175, 28.6.01, p.21.
O.J. No. L 176, 29.6.01, p.61.
O.J. No. L 276, 19.10.01, p.17.
O.J. No. L 304, 21.11.01, p.14.
O.J. No. L 313, 30.11.01, p.37.
O.J. No. L 55, 26.2.02, p.29.
O.J. No. L 117, 4.5.02, p.10.
O.J. No. L 148, 6.6.02, p.19.
O.J. No. L 189, 18.7.02, p.27.
O.J. No. L 276, 12.10.02, p.28.
O.J. No. L 8, 14.1.03, p.7.
O.J. No. L 81, 28.3.03, p.39.
O.J. No. L 177, 16.7.03, p.12.
O.J. No. L 228, 12.9.03, p.11.
O.J. No. L 101, 23.4.03, p.3.
O.J. No. L 205, 14.8.03, p.16.
O.J. No. L 247, 30.9.03, p.20.
O.J. No. L 124, 20.5.03, p.30.
O.J. No. L 184, 23.7.03, p.9.
O.J. No. L 224, 6.9.03, p.29.
O.J. No. L 196, 16.8.67, p.1 (O.J./SE 1967 p.234).
Last amended by Council Regulation (EC) No. 806/2003 (O.J. No. L 122, 16.5.03, p.1).
O.J. No. L 200, 30.7.99, p.1.
Amended by Commission Directive 2001/60/EC (O.J. No. L 226, 22.8.01, p.5).
By J Rigaudy and S P Klesney, published by Pergamon (ISBN 0-08022-3699).
By R Panico, W H Powell and J-C Richer, published by Blackwell Science (ISBN 0-63203-4882). Corrections published in Pure Appl. Chem., vol. 71, No. 7, pp. 1327-1330, 1999.