Northern Ireland Statutory Rule 2001 United Kingdom

Biocidal Products Regulations (Northern Ireland) 2001

At a glance

What's here

1 compliance obligation

What this Act requires

Sections that create concrete duties on businesses or carry penalties. Procedural and definitional sections are folded into the “Browse other sections” expander at the bottom of each group. Click any section title to read the source text on legislation.gov.uk.

Schedules

Browse 113 other Schedules — structural / supplementary
s.sch003

Subject to paragraph 2, the Executive has determined that the...

s.sch003

In making the determinations referred to in paragraph 1, the...

s.sch003

The Executive has determined, according to the relevant requirements in...

s.sch003

The Executive has 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 Executive 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

Interpretation

s.sch010

Application of the Health and Safety at Work (Northern Ireland) Order 1978

s.sch010

Offences

s.sch010

Limitation on entry to domestic premises in certain circumstances

s.sch010

Allocation of enforcement responsibility

s.sch011

On the making of an application to the Executive under...

s.sch011

If the cost referred to in paragraph 9 is greater...

s.sch011

If the cost referred to in paragraph 9 is less...

s.sch011

In estimating or stating the cost of carrying out any...

s.sch011

There shall be payable by the applicant to the Executive...

s.sch011

The applications to the Executive referred to in paragraph 2...

s.sch011

There shall be payable by the applicant to the Executive...

s.sch011

There shall be payable by a person who provides information...

s.sch011

There shall be payable by a person who requests a...

s.sch011

On receipt of— (a) an application referred to in paragraph...

s.sch011

The amount estimated in accordance with paragraph 7 shall be...

s.sch011

On the determination of the application, completion of the evaluation...

s.sch012

In this Schedule— “COPR 1987” means the Control of Pesticides...

s.sch012

Where— (a) no application is made in accordance with paragraph...

s.sch012

Where— (a) an application is made in accordance with paragraph...

s.sch012

Where— (a) there is made a decision referred to in...

s.sch012

Where— (a) there is made a decision referred to in...

s.sch012

The Executive shall— (a) notify in writing the holder of...

s.sch012

A certificate of exemption granted pursuant to paragraph 6, 7,...

s.sch012

An exemption certificate granted in accordance with paragraph 15—

s.sch012

Subject to paragraphs 3 and 4, where a decision is...

s.sch012

These Regulations shall not apply to a biocidal product—

s.sch012

Where there is more than one unlisted active substance in...

s.sch012

Where— (a) there is made a decision referred to in...

s.sch012

Where— (a) there is made a decision referred to in...

s.sch012

During— (a) the period of time in which an application...

s.sch012

Where— (a) there is made a decision referred to in...

s.sch012

During— (a) the period of time in which an application...

s.sch013

Interpretation

s.sch013

Offshore installations

s.sch013

Wells

s.sch013

Pipelines

s.sch013

Mines

s.sch013

Other activities

s.025

Co-operation in the use of information

  • Check with Executive before testing on vertebrate animals
Browse 41 other sections — procedural / definitional / commencement
s.001

Citation and commencement

s.002

Interpretation

s.003

Application

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

s.008

Prohibitions

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.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 Poison Information Service

s.030

Packaging

s.031

Labelling

s.032

Samples, models and drafts

s.033

Advertisements

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

Application within territorial waters

s.042

Amendments

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