- Latest available (Revised)
- Point in Time (31/12/2020)
- Original (As made)
The Plant Protection Products (Fees and Charges) Regulations 2011
You are here:
- UK Statutory Instruments
- 2011 No. 2132
- Explanatory Note
What Version
Advanced Features
- Show Geographical Extent(e.g. England, Wales, Scotland and Northern Ireland)
- Show Timeline of Changes
More Resources
Changes over time for: Explanatory Notes
Alternative versions:
- 24/09/2011- Amendment
- 31/12/2020
Point in time
Status:
Point in time view as at 31/12/2020.
Changes to legislation:
There are outstanding changes not yet made by the legislation.gov.uk editorial team to The Plant Protection Products (Fees and Charges) Regulations 2011. Any changes that have already been made by the team appear in the content and are referenced with annotations.
Changes to Legislation
Changes and effects yet to be applied by the editorial team are only applicable when viewing the latest version or prospective version of legislation. They are therefore not accessible when viewing legislation as at a specific point in time. To view the ‘Changes to Legislation’ information for this provision return to the latest version view using the options provided in the ‘What Version’ box above.
EXPLANATORY NOTE
(This note is not part of the Regulations)
1. These Regulations provide the charging regime in relation to—U.K.
(a)Regulation (EC) No 1107/2009 of the European Parliament and of the Council of 21 October 2009 concerning the placing of plant protection products on the market and repealing Council Directives 79/117/EEC and 91/414/EEC (OJ No L309, 24.11.2009, p.1) (“Regulation 1107/2009”);
(b)Regulation (EC) No 396/2005 of the European Parliament and of the Council of 23 February 2005 on maximum residue levels of pesticides in or on food and feed of plant and animal origin and amending Council Directive 91/414/EEC (OJ No L70, 16.3.2005, p.1) (“the MRL Regulation”); and
(c)Directive 2009/128/EC of the European Parliament and of the Council of 21 October 2009 establishing a framework for Community action to achieve the sustainable use of pesticides (OJ No L 4, 6. 1. 96, p.16) (“the Directive”).
2. Regulation 1107/2009 replaces the existing scheme for approval under Council Directive 91/414/EEC concerning the placing of plant protection products on the market (OJ No L230, 19.8.1991, p.1), and lays down rules for the approval of active substances and the authorisation of plant protection products.U.K.
3. These Regulations set fees, chargeable by the Secretary of State, the Scottish Ministers and the Department of Agriculture and Rural Development in Northern Ireland (“the United Kingdom competent authorities”) for—U.K.
(a)work carried out within the scope of Regulation 1107/2009 which relates to evaluating applications for the authorisation of plant protection products, the approval of active substances, safeners, synergists and basic substances and official recognition of a test facility or organisation, and
(b)applications for import tolerances under Article 7 of the MRL Regulation.
4. These Regulations also provide for an annual charge to be paid by authorisation holders for costs incurred by or on behalf of the United Kingdom competent authorities associated with any work carried out within the scope of Regulation 1107/2009 and work arising from the obligations under the MRL Regulation (other than for work charged under section 18(2)(b) or (c) of the Food and Environment Protection Act 1985) and, after 26th November 2011, work pursuant to obligations within the scope of the Directive. These Regulations also set out the consequences of failure to pay fees or charges.U.K.
5. These Regulations revoke and replace—U.K.
(a)The Fees for Assessment of Active Substances (Third Stage Review) Regulation 2005 (S.I. 2005/117);
(b)The Fees for Assessment of Active Substances (Fourth Stage Review) Regulation 2005 (S.I. 2005/1811); and
(c)the Plant Protection Products (Fees) Regulations 2007(S.I. 2007/295).
6. A full regulatory impact assessment of the effect that this instrument will have on the costs to business and the voluntary sector has also been prepared. A copy of this document has been placed in the library of each House of Parliament and is available on DEFRA’s website (www.defra.gov.uk). A copy of the regulatory impact assessment is also annexed to the Explanatory Memorandum to the Plant Protection Products Regulations 2011 and to these Regulations and is available alongside the instruments on the legislation website (http://www.legislation.gov.uk/).U.K.
7. The new fees compared with those fixed by or determined under the previous fee-charging provisions are as follows:U.K.
| Type of Fee | Previous Fee (£) | New Fee (£) | Percentage Increase/Decrease | |
|---|---|---|---|---|
| Schedule 1 | ||||
| 1. Product related applications | ||||
1.— U.K. | Administrative research and development application | 30.00 | 50.00 | 66.67% |
2.— U.K. | Extension of use application including administration, co-ordination and technical consideration | 1,495.00 | 1,495.00 | 0.00% |
Extension of use application from 1 April 2012 | 1,495.00 | 1,700.00 | 13.71% | |
3.— U.K. | Preliminary consideration of application type listed in item 4, 5, 7, 12 or 13, to determine whether the application can proceed further | 150.00 (electronic) or 175.00 (other) | 220.00 | 46.67% or 25.71% |
4.— U.K. | Administrative application for a new product or change to an existing product, | |||
(a) | One product | 120.00 | 150.00 | 25.00% |
(b) | Each additional product | 40.00 | 50.00 | 25.00% |
5.— U.K. | Parallel trade application; | |||
(a) | Co-ordination of application for new product or change to existing product involving parallel trade | 710.00 | 700.00 | -1.41% |
(b) | Parallel trade verification | 200.00 | 200.00 | 0.00% |
6.— U.K. | Evaluation of a label in any application. | 300.00 | 200.00 | -33.33% |
7.— U.K. | Coordination of standard technical stream application | 1,100.00 (technical) or 1,800.00 (data evaluation) | 1,800.00 | 45.45% or 0.00% |
8.— U.K. | Evaluation of simple reasoned cases in each of the following specialist areas: | |||
(a) | Chemistry | 250.00 | 400.00 | 60.00% |
(b) | Toxicology | 250.00 | 400.00 | 60.00% |
(c) | Operator exposure | 250.00 | 400.00 | 60.00% |
(d) | Residues/consumer exposure | 250.00 | 400.00 | 60.00% |
(e) | Fate and behaviour in the environment | 250.00 | 400.00 | 60.00% |
(f) | Ecotoxicology | 250.00 | 400.00 | 60.00% |
(g) | Efficacy | 250.00 | 400.00 | 60.00% |
9.— U.K. | Evaluation of data, modelling and detailed scientific cases in each of the following specialist areas: | |||
(a) | Chemistry | 425.00 | 750.00 | 76.47% |
(b) | Toxicology | 500.00 | 750.00 | 50.00% |
(c) | Operator exposure | 750.00 | 750.00 | 0.00% |
(d) | Residues/consumer exposure | 1,000.00 | 750.00 | -25.00% |
(e) | Fate and behaviour in the environment | 1,000.00 | 1,800.00 | 80.00% |
(f) | Ecotoxicology | 1,000.00 | 1,800.00 | 80.00% |
(g) | Efficacy | 1,500.00 | 1,800.00 | 20.00% |
Crop Safety (£500) and Effectiveness (£1000) previously charged separately | ||||
10.— U.K. | Withdrawal of an application for a product specified in items 2, 4, 5, 7, 12 or 13 before any work other than preliminary consideration has been done | 100.00 | 100.00 | 0.00% |
11.— U.K. | Pre-submission meetings for lead zone re-registration and new product applications | 0.00 | 5,000.00 | New item |
12.— U.K. | Zonal surcharges for lead zonal re-registration and new product applications. This fee is in addition to these described in 7 to 9 above | |||
Zonal surcharge 1 | 0.00 | 7,500.00 | New item | |
Zonal surcharge 2 | 0.00 | 15,000.00 | New item | |
13.— U.K. | Commenting on draft study protocols | 0.00 | 400.00 | New item |
| 2. Active substances related applications | ||||
| Where an active substance, safener or synergist is neither a biocontrol agent nor a pheromone | ||||
1.— U.K. | Preliminary evaluation of an application’s admissibility | 5,000.00 | 5,000.00 | 0.00% |
2.— U.K. | Processing an application for provisional authorisation | 35,000.00 | 35,000.00 | 0.00% |
3.— U.K. | Helping the European Food Safety Authority to evaluate the draft assessment report where the United Kingdom is the rapporteur or co-rapporteur member state | 35,000.00 | 35,000.00 | 0.00% |
4.— U.K. | Evaluation of a full data package | 105,000.00 | 110,00.00 | 4.76% |
5.— U.K. | Evaluation of a partial data package: | |||
Band 1 | 7,500.00 | New item | ||
Band 2 | 15,000.00 | 15,000.00 | 0.00% | |
Band 3 | 30,000.00 | 30,000.00 | 0.00% | |
Band 4 | 40,000.00 | 50,000.00 | 25.00% | |
Band 5 | 60,000.00 | 70,000.00 | 16.67% | |
Band 6 | 80,000.00 | 90,000.00 | 12.50% | |
Band 7 | 105,000.00 | 110,000.00 | 4.76% | |
| Where an active substance is a biocontrol agent | ||||
6.— U.K. | Evaluation of a full data package | 22,500.00 | 22,500.00 | 0.00% |
7.— U.K. | Helping the European Food Safety Authority to evaluate the draft assessment report where the United Kingdom is the rapporteur or co-rapporteur member State | 7,500.00 | 7,500.00 | 0.00% |
8.— U.K. | Evaluation of a partial data package: | |||
Band 1 | 5,500.00 | 5,500.00 | 0.00% | |
Band 2 | 11,250.00 | 11,250.00 | 0.00% | |
Band 3 | 17,000.00 | 17,000.00 | 0.00% | |
Band 4 | 22,500.00 | 22,500.00 | 0.00% | |
| Where an active substance is a pheromone | ||||
9.— U.K. | Evaluation of a fill data package | 13,000.00 | 13,000.00 | 0.00% |
10.— U.K. | Helping the European Food Safety Authority to evaluate the draft assessment report where the United Kingdom is a rapporteur or co-rapporteur member State. | 7,500.00 | 7,500.00 | 0.00% |
11.— U.K. | Evaluation of a partial data package: | |||
Band 1 | 3,250.00 | 3,250.00 | 0.00% | |
Band 2 | 6,500.00 | 6,500.00 | 0.00% | |
Band 3 | 9,750.00 | 9,750.00 | 0.00% | |
Band 4 | 13,000.00 | 13,000.00 | 0.00% | |
| For all evaluations | ||||
12.— U.K. | Meeting before the submission of an application in support of new active substance, safener or synergist, biocontrol and pheromone applications | 0.00 | 5,000.00 | New item |
| 3. Fees for official recognition of a test facility or organisation | ||||
Initial official recognition of the test facility | 1,500.00 | 2,000.00 | 33.33% | |
Renewal of an official recognition | 1,500.00 | 2,000.00 | 33.33% | |
Each re-inspection | 1,125.00 | 1,500.00 | 33.33% | |
| 4. Basic substance applications | ||||
1.— U.K. | Assistance with a full data package | 0.00 | 110,000.00 | New item |
2.— U.K. | Assistance with a partial data package: | |||
Band 1 | 0.00 | 7,500.00 | New item | |
Band 2 | 0.00 | 15,000.00 | New item | |
Band 3 | 0.00 | 30,000.00 | New item | |
Band 4 | 0.00 | 50,000.00 | New item | |
Band 5 | 0.00 | 70,000.00 | New item | |
Band 6 | 0.00 | 90,000.00 | New item | |
Band 7 | 0.00 | 110,000.00 | New item | |
| Schedule 2 | ||||
| Import tolerance fee | ||||
1.— U.K. | Full human health evaluation | 15,600.00 | 15,600.00 | 0.00% |
2.— U.K. | Metabolism and residues evaluation | 6,500.00 | 6,500.00 | 0.00% |
3.— U.K. | Residues evaluation | 1,950.00 | 1,950.00 | 0.00% |
Options/Help
Print Options
PrintThe Whole Instrument
PrintThis Explanatory Note only
Legislation is available in different versions:
Latest Available (revised):The latest available updated version of the legislation incorporating changes made by subsequent legislation and applied by our editorial team. Changes we have not yet applied to the text, can be found in the ‘Changes to Legislation’ area.
Original (As Enacted or Made): The original version of the legislation as it stood when it was enacted or made. No changes have been applied to the text.
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.
See additional information alongside the content
Geographical Extent: Indicates the geographical area that this provision applies to. For further information see ‘Frequently Asked Questions’.
Show Timeline of Changes: See how this legislation has or could change over time. Turning this feature on will show extra navigation options to go to these specific points in time. Return to the latest available version by using the controls above in the What Version box.
Opening Options
Different options to open legislation in order to view more content on screen at once
Explanatory Memorandum
Explanatory Memorandum sets out a brief statement of the purpose of a Statutory Instrument and provides information about its policy objective and policy implications. They aim to make the Statutory Instrument accessible to readers who are not legally qualified and accompany any Statutory Instrument or Draft Statutory Instrument laid before Parliament from June 2004 onwards.
More Resources
Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:
- the original print PDF of the as enacted version that was used for the print copy
- lists of changes made by and/or affecting this legislation item
- confers power and blanket amendment details
- all formats of all associated documents
- correction slips
- links to related legislation and further information resources
Impact Assessments
Impact Assessments generally accompany all UK Government interventions of a regulatory nature that affect the private sector, civil society organisations and public services. They apply regardless of whether the regulation originates from a domestic or international source and can accompany primary (Acts etc) and secondary legislation (SIs). An Impact Assessment allows those with an interest in the policy area to understand:
- Why the government is proposing to intervene;
- The main options the government is considering, and which one is preferred;
- How and to what extent new policies may impact on them; and,
- The estimated costs and benefits of proposed measures.
Timeline of Changes
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.
More Resources
Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:
- the original print PDF of the as made version that was used for the print copy
- correction slips
Click 'View More' or select 'More Resources' tab for additional information including:
- lists of changes made by and/or affecting this legislation item
- confers power and blanket amendment details
- all formats of all associated documents
- links to related legislation and further information resources
All content is available under the Open Government Licence v3.0 except where otherwise stated. This site additionally contains content derived from EUR-Lex, reused under the terms of the Commission Decision 2011/833/EU on the reuse of documents from the EU institutions. For more information see the EUR-Lex public statement on re-use.