- Enforced by
- HSE
- Status
- Amended (in force with amendments)
- Penalty ceiling
- Regulated
Does it bind you?
Business-side roles with duties under this instrument.
Applicant1
Plus 1 duty on the regulator, Crown ministers and public bodies — folded into the section list below.
Other Acts binding the same actors
If a role above is yours, these are the other instruments that most often bind it.
Applicant — also bound by 307 other Acts
Human Medicines Regulations 2012
42 duties
The Land Registration Rules 2003
25 duties
Regulation (EU) No 1178/2011 (Aircrew)
20 duties
Value Added Tax Regulations 1995
18 duties
What it requires
Regulations creating concrete business duties or carrying penalties, grouped as the instrument is structured. Titles link to the source text — blue means you’re leaving for legislation.gov.uk.
Part 1
GENERAL
0 of 3 sections shown3 other sections in this Part — procedural and definitional
s.001
Citation and commencement
s.002
Interpretation
s.003
Application
Part 2
ACTIVE SUBSTANCES
0 of 4 sections shown4 other sections in this Part — procedural and definitional
s.004
Placing on the market of active substances
s.005
Applications concerning new active substances
s.006
Assessment of applications concerning new active substances
s.007
Applications for variation or renewal of the inclusion of active substances in Annex I, IA or IB
Part 3
BIOCIDAL PRODUCTS
0 of 15 sections shown15 other sections in this Part — procedural and definitional
s.009
Authorisation of a biocidal product
s.010
Registration of a low-risk biocidal product
s.011
Mutual recognition of authorisations
s.012
Mutual recognition of registrations
s.013
Provisional authorisation
s.014
Provisional registration
s.015
Emergency authorisation
s.016
Research and development
s.017
Experimental authorisation
s.018
Frame-formulations
s.019
Revocation of authorisations and registrations
s.020
Modification and review of authorisations and registrations
s.021
Notification of new information
s.022
Emergency prohibition or restriction
s.part iii/regulation/8
Prohibitions
Part 4
USE OF INFORMATION
1 of 7 sections shown
s.025
Co-operation in the use of information
Regulated
- New applicants must check for existing product data before animal testingApplicant
6 other sections in this Part — procedural and definitional
s.023
Data protection for active substances
s.024
Data protection for biocidal products
s.026
Confidentiality
s.027
Treatment of confidential information
s.028
Exchange of information
s.029
Notification of information to the National Poisons Information Service
Part 5
PACKAGING, LABELLING AND ADVERTISEMENTS
0 of 4 sections shown4 other sections in this Part — procedural and definitional
s.030
Packaging
s.031
Labelling
s.032
Samples, models and drafts
s.033
Advertisements
Part 6
MISCELLANEOUS AND GENERAL
0 of 10 sections shown10 other sections in this Part — procedural and definitional
s.034
General provisions on applications for authorisations and registrations
s.035
Files on applications
s.036
Appeals
s.037
Tests
s.038
Enforcement, offences and civil liability
s.039
Fees
s.040
Transitional provisions
s.041
Extension outside Great Britain
s.042
Amendments
s.part vi/regulation/8
In this regulation, “the appropriate person” means—
Schedules
Schedules
1 of 120 shown
s.sch010
(1) Where a government department has expressed in writing to...
Regulated
Other duties (1) — Crown / regulator
- Ministers must make a government department representative available as a witness at appeal hearingsCrown / Minister / Government department
119 other schedules
s.sch003
Subject to paragraph 2, the Ministers have determined that the...
s.sch003
In making the determinations referred to in paragraph 1, the...
s.sch003
The Ministers have determined, according to the relevant requirements in...
s.sch003
The Ministers have determined— (a) the physical and chemical properties...
s.sch004
The name and address of the applicant.
s.sch004
Efficacy data.
s.sch004
Analytical methods.
s.sch004
The classification, packaging and labelling of the biocidal product, including...
s.sch004
Where the biocidal product is a substance or preparation dangerous...
s.sch004
The name and address of the manufacturer of the biocidal...
s.sch004
The name and address of the manufacturer of the active...
s.sch004
The trade name of the biocidal product.
s.sch004
The name of each substance in the biocidal product, including...
s.sch004
The physical and chemical properties of the biocidal product relating...
s.sch004
The product-type and field of use of the biocidal product....
s.sch004
The intended category of users.
s.sch004
The intended method of use.
s.sch005
Directions for use of the biocidal product in question, including...
s.sch005
Particulars of any likely direct or indirect adverse side effects...
s.sch005
Directions for safe disposal of the biocidal product in question...
s.sch005
The period of time needed for the biocidal effect.
s.sch005
The interval to be observed between— (a) applications of the...
s.sch005
Particulars for adequate cleaning of equipment.
s.sch005
Particulars concerning precautionary measures during use, storage and transport, such...
s.sch005
Information on any specific dangers to the environment, including protection...
s.sch006
The name and address of the applicant for the authorisation...
s.sch006
Recommended methods and precautions to reduce dangers from handling, storage,...
s.sch006
Safety data sheets.
s.sch006
Methods of analysis necessary to enable the Ministers to make...
s.sch006
Methods of disposal of the biocidal product and its packaging....
s.sch006
Procedures to be followed and measures to be taken in...
s.sch006
First aid and medical advice to be given in the...
s.sch006
The name of the biocidal product.
s.sch006
The name and address of the manufacturer of the biocidal...
s.sch006
The name and address of the manufacturer of the active...
s.sch006
The name and content of the active substance in the...
s.sch006
The name of any other substance in the biocidal product...
s.sch006
Physical and chemical data concerning the biocidal product and the...
s.sch006
Any ways of rendering harmless the biocidal product and the...
s.sch006
A summary of the results of the tests, referred to...
s.sch007
The name of the applicant for, or the person to...
s.sch007
Whether the biocidal product is a low-risk biocidal product or...
s.sch007
The trade name of the biocidal product.
s.sch007
The name and amount of each active substance which the...
s.sch007
The name and amount of each substance which the biocidal...
s.sch007
The product-type for the biocidal product and the use for...
s.sch007
The type of formulation of the biocidal product, namely whether...
s.sch007
Any proposed limits on residues which have been determined by...
s.sch007
Any conditions subject to which the authorisation or registration was...
s.sch007
The reasons for the modification or cancellation of an authorisation...
s.sch008
The name of the biocidal product.
s.sch008
Any other information relating to the health and safety of...
s.sch008
If the biocidal product is authorised or registered under these...
s.sch008
The date on which the biocidal product was first placed...
s.sch008
The name, address and telephone number and any e-mail address...
s.sch008
A description of the packaging of the biocidal product, including...
s.sch008
The pH, physical state and colour of the biocidal product....
s.sch008
The identity of the ingredients of the biocidal product, and...
s.sch008
The effects on human health of contact with the biocidal...
s.sch008
Particulars of the likely direct or indirect adverse side effects...
s.sch009
The identity of the active substance in the biocidal product...
s.sch009
The interval to be observed between— (a) applications of the...
s.sch009
Instructions for adequate cleaning of equipment for use with the...
s.sch009
Instructions concerning precautionary measures during use, storage and transport, such...
s.sch009
Any restriction on the category of persons who may use...
s.sch009
Information on any specific dangers to the environment, including protection...
s.sch009
The authorisation or registration number allocated to the biocidal product...
s.sch009
The type of formulation of the biocidal product, namely whether...
s.sch009
The use for which the biocidal product is authorised or...
s.sch009
Directions for use of the biocidal product, including its dose...
s.sch009
Particulars of likely direct or indirect adverse side effects and...
s.sch009
Directions for safe disposal of the biocidal product and its...
s.sch009
The number or other reference assigned by the manufacturer of...
s.sch009
The period of time needed for the biocidal effect.
s.sch010
In this Schedule— (a) “appeal” means an appeal under regulation...
s.sch010
(1) Except as otherwise provided in this Part of this...
s.sch010
(1) Where, after the close of the hearing, the appointed...
s.sch010
The appointed person shall notify the determination on the appeal,...
s.sch010
The appropriate person shall direct that an appeal shall be...
s.sch010
Before the determination of an appeal, the appointed person shall...
s.sch010
An appointed person may give such directions as he thinks...
s.sch010
The appropriate person may pay to an appointed person such...
s.sch010
An appeal brought pursuant to regulation 36(1)(j) shall be heard...
s.sch010
(1) Subject to the following sub-paragraphs of this paragraph, a...
s.sch010
(1) Not later than 28 days before the date of...
s.sch010
(1) The parties shall be entitled to appear at the...
s.sch011
Interpretation
s.sch011
Application of the
s.sch011
Offences
s.sch011
Limitation on entry to domestic premises in certain circumstances
s.sch011
Allocation of enforcement responsibility
s.sch012
On the making of an application to the Ministers under...
s.sch012
If the cost referred to in paragraph 9 is greater...
s.sch012
If the cost referred to in paragraph 9 is less...
s.sch012
In estimating or stating the cost of carrying out any...
s.sch012
There shall be payable by the applicant to the Ministers...
s.sch012
The applications to the Ministers referred to in paragraph 2...
s.sch012
There shall be payable by the applicant to the Ministers...
s.sch012
There shall be payable by a person who provides information...
s.sch012
There shall be payable by a person who requests a...
s.sch012
On receipt of— (a) an application referred to in paragraph...
s.sch012
The amount estimated in accordance with paragraph 7 shall be...
s.sch012
On the determination of the application, completion of the evaluation...
s.sch013
In this Schedule— “COPR 1986” means the Control of Pesticides...
s.sch013
Where— (a) no application is made in accordance with paragraph...
s.sch013
Where— (a) an application is made in accordance with paragraph...
s.sch013
Where— (a) there is made a decision referred to in...
s.sch013
Where— (a) there is made a decision referred to in...
s.sch013
The Ministers shall— (a) notify in writing the holder of...
s.sch013
A certificate of exemption granted pursuant to paragraph 6, 7,...
s.sch013
An exemption certificate granted in accordance with paragraph 15—
s.sch013
Subject to paragraphs 3 and 4, where a decision is...
s.sch013
These Regulations shall not apply to a biocidal product—
s.sch013
Where there is more than one unlisted active substance in...
s.sch013
Where— (a) there is made a decision referred to in...
s.sch013
Where— (a) there is made a decision referred to in...
s.sch013
During— (a) the period of time in which an application...
s.sch013
Where— (a) there is made a decision referred to in...
s.sch013
During— (a) the period of time in which an application...
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