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Biocidal Products Regulations (Northern Ireland) 2001

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  1. Introductory Text

  2. Part I General

    1. 1.Citation and commencement

    2. 2.Interpretation

    3. 3.Application

  3. Part II Active Substances

    1. 4.Placing on the market of active substances

    2. 5.Applications concerning new active substances

    3. 6.Assessment of applications concerning new active substances

    4. 7.Applications for variation or renewal of the inclusion of active substances in Annex I, IA or IB

  4. Part III Biocidal Products

    1. 8.Prohibitions

    2. 9.Authorisation of a biocidal product

    3. 10.Registration of a low-risk biocidal product

    4. 11.Mutual recognition of authorisations

    5. 12.Mutual recognition of registrations

    6. 13.Provisional authorisation

    7. 14.Provisional registration

    8. 15.Emergency authorisation

    9. 16.Research and development

    10. 17.Experimental authorisation

    11. 18.Frame-formulations

    12. 19.Revocation of authorisations and registrations

    13. 20.Modification and review of authorisations and registrations

    14. 21.Notification of new information

    15. 22.Emergency prohibition or restriction

  5. Part IV Use of Information

    1. 23.Data protection for active substances

    2. 24.Data protection for biocidal products

    3. 25.Co-operation in the use of information

    4. 26.Confidentiality

    5. 27.Treatment of confidential information

    6. 28.Exchange of information

    7. 29.Notification of information to the Poison Information Service

  6. Part V Packaging, Labelling and Advertisements

    1. 30.Packaging

    2. 31.Labelling

    3. 32.Samples, models and drafts

    4. 33.Advertisements

  7. Part VI Miscellaneous and General

    1. 34.General provisions on applications for authorisations and registrations

    2. 35.Files on applications

    3. 36.Appeals

    4. 37.Tests

    5. 38.Enforcement, offences and civil liability

    6. 39.Fees

    7. 40.Transitional provisions

    8. 41.Application within territorial waters

    9. 42.Amendments

  8. Signature

  9. SCHEDULES

    1. Schedule 1

      Biocidal product types and their descriptions.

    2. Schedule 2

      Regulations relating to biocidal products.

    3. Schedule 3

      Determinations of the Executive.

    4. Schedule 4

      Information to be contained in a dossier submitted in support of an application for the registration of a biocidal product.

    5. Schedule 5

      Matters in respect of which additional conditions may be imposed on the mutual recognition of an authorisation or a registration of a biocidal product.

    6. Schedule 6

      Non-confidential information.

    7. Schedule 7

      Information relating to biocidal products to be given to the Commission and to the competent authorities.

    8. Schedule 8

      Information to be notified to the Poison Information Service.

    9. Schedule 9

      Information to be included on labels.

    10. Schedule 10

      Enforcement, offences and civil liability.

    11. Schedule 11

      Fees.

    12. Schedule 12

      Transitional provisions.

    13. Schedule 13

      Application within territorial waters.

  10. Explanatory Note

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